A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661685



Internal ID9927790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29883595..29938447hg38UCSC Ensembl
chr6:29851372..29906224hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3854853
hg1954853
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1087e199
Supporting Variantsessv5543836, essv6259920, essv5626522, essv6004651, essv5611820, essv6547799, essv5969204, essv6427470, essv5806196, essv6403855, essv6032905, essv5452828, essv5690251, essv5418628, essv6085656, essv5927440, essv6083085, essv5662069, essv5999862, essv6130907, essv6032003, essv5736272, essv6284518, essv5674109
SamplesHG01441, HG01356, HG01389, HG01461, HG01140, HG01250, HG01350, HG01488, HG01492, HG01365, HG01455, HG01495, HG01550, HG01124, HG01353, HG01498, HG01497, HG01494, HG01113, HG00378, HG01251, HG01378, HG01125, HG01437
Known GenesHCG4B, HLA-H
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661685
Frequency
Sample Size1151
Observed Gain0
Observed Loss24
Observed Complex0
Frequencyn/a


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