A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697444



Internal ID15434096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:142547962..142587009hg38UCSC Ensembl
Innerchr6:142869099..142908146hg19UCSC Ensembl
Innerchr6:142910792..142949839hg18UCSC Ensembl
Innerchr6:142910792..142949839hg17UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3839048
hg1939048
hg1839048
hg1739048
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520479
Supporting Variants
Samples
Known GenesLOC153910
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697444
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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