A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670007



Internal ID9589426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159934669..159934817hg38UCSC Ensembl
chr6:160355701..160355849hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5870708, essv5953575, essv6014176, essv6033114, essv6579822, essv5703449, essv5832586, essv5829471, essv5445954, essv6288081, essv6282478, essv6024426, essv6576624, essv6550412, essv6155689, essv5831777, essv5659620, essv5485998, essv6363092, essv5815161, essv5423720, essv5490909, essv5759124
SamplesHG01356, HG01465, HG01456, NA12155, NA07357, HG01350, NA11992, HG00185, HG01134, HG00326, NA20524, NA20521, HG01095, NA12234, HG00284, HG01107, HG00237, NA20504, HG00342, NA20528, HG00345, NA20585, NA12154
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670007
Frequency
Sample Size1151
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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