A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611609



Internal ID6998515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:164949371..164959531hg38UCSC Ensembl
Innerchr6:164949371..164959531hg38UCSC Ensembl
Outerchr6:164948871..164960031hg38UCSC Ensembl
chr6:165362860..165373020hg19UCSC Ensembl
Innerchr6:165362860..165373020hg19UCSC Ensembl
Outerchr6:165362360..165373520hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3810161
hg1910161
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12627438, essv12627437, essv12627435, essv12627436
SamplesHG02014, HG02497, HG03565, HG03442
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611609
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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