A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12608411



Internal ID2610227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:158971725..158973715hg38UCSC Ensembl
Innerchr6:158971741..158973700hg38UCSC Ensembl
Outerchr6:158971710..158973731hg38UCSC Ensembl
chr6:159392757..159394747hg19UCSC Ensembl
Innerchr6:159392773..159394732hg19UCSC Ensembl
Outerchr6:159392742..159394763hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg381991
hg191991
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3611410
Supporting Variants
SamplesNA19090
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12608411
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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