A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678587



Internal ID9944692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174095064..174095867hg38UCSC Ensembl
chr4:175016215..175017018hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38804
hg19804
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5581043, essv6388804, essv6303490, essv6378477, essv6577736, essv6593395, essv6280662, essv6512291, essv5686622, essv6474476, essv5961774, essv6317575, essv5473633, essv6478098, essv6268400, essv5806290, essv6342334, essv5695472, essv6216776, essv5574065, essv5563892, essv5773886, essv5605343, essv5560736, essv6077408, essv6153201, essv5752744, essv6427217, essv6404026, essv5902293, essv6497874, essv5845155, essv6336599, essv6008573, essv6065729, essv5919130, essv6487319, essv5423250
SamplesHG01441, HG01356, HG01462, HG01359, HG01389, HG01374, HG01465, HG01456, HG01461, HG01140, HG01350, HG01366, HG01351, HG01488, HG01492, HG01354, HG01365, HG01134, HG01440, HG01124, HG01353, HG01136, HG01384, HG01498, HG01149, HG01390, HG01497, HG01148, HG01357, HG01375, 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)esv2678587
Frequency
Sample Size1151
Observed Gain0
Observed Loss38
Observed Complex0
Frequencyn/a


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