A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677588



Internal ID9597007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:158803151..158803512hg38UCSC Ensembl
Outerchr6:158802994..158803665hg38UCSC Ensembl
Innerchr6:159224183..159224544hg19UCSC Ensembl
Outerchr6:159224026..159224697hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38672
hg19672
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1164e199
Supporting Variantsessv6544219, essv6579874, essv6539012
SamplesNA18867, HG00246, NA19380
Known GenesEZR
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677588
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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