A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703729



Internal ID15440381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:85114605..85117806hg38UCSC Ensembl
Innerchr6:85824323..85827524hg19UCSC Ensembl
Innerchr6:85881042..85884243hg18UCSC Ensembl
Innerchr6:85881042..85884243hg17UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg383202
hg193202
hg183202
hg173202
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520873
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703729
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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