A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608675



Internal ID6995599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35041198..35043842hg38UCSC Ensembl
Innerchr6:35041198..35043842hg38UCSC Ensembl
Outerchr6:35041028..35043975hg38UCSC Ensembl
chr6:35008975..35011619hg19UCSC Ensembl
Innerchr6:35008975..35011619hg19UCSC Ensembl
Outerchr6:35008805..35011752hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg382645
hg192645
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12315482
SamplesHG02582
Known GenesANKS1A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608675
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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