A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610844



Internal ID6651070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132754654..132762349hg38UCSC Ensembl
Innerchr6:132754654..132762349hg38UCSC Ensembl
Outerchr6:132754407..132762499hg38UCSC Ensembl
chr6:133075793..133083488hg19UCSC Ensembl
Innerchr6:133075793..133083488hg19UCSC Ensembl
Outerchr6:133075546..133083638hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg387696
hg197696
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1219e214
Supporting Variantsessv12554761, essv12554760
SamplesHG03784, HG03786
Known GenesVNN2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610844
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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