A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664993



Internal ID9931098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:11444992..11445498hg38UCSC Ensembl
Outerchr4:11444621..11445868hg38UCSC Ensembl
Innerchr4:11446616..11447122hg19UCSC Ensembl
Outerchr4:11446245..11447492hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg381248
hg191248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5925599, essv5463984, essv6090129, essv5453621, essv6526086, essv5644671, essv5730292, essv5680050, essv5985747, essv6186929, essv6028772, essv5474979, essv6267730, essv5720257, essv6235412, essv5414102, essv5840653, essv5814655, essv6394131, essv6383823, essv6247556, essv5874773, essv6285886, essv6145379, essv6510875, essv5774671, essv6289521, essv6246815, essv6018446, essv5433134, essv5850583, essv6351811, essv5837718, essv5640704, essv6256213, essv5598765, essv6233858, essv5505116, essv6413523, essv5404778
SamplesHG01441, HG01356, HG01462, HG01359, HG01389, HG01374, HG01465, HG01461, HG01140, HG01350, HG01366, HG01351, HG01488, HG01492, HG01365, HG01134, HG01440, HG01124, HG01353, HG01136, HG01360, HG01384, HG01149, HG01390, HG01383, HG01497, HG01148, HG01253, HG01357, HG01375, HG01494, HG01113, HG01137, HG01489, HG01342, HG01491, HG01377, HG01378, HG01125, HG01437
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664993
Frequency
Sample Size1151
Observed Gain0
Observed Loss40
Observed Complex0
Frequencyn/a


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