A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694677



Internal ID15431329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:153691006..153698695hg38UCSC Ensembl
Innerchr3:153408795..153416484hg19UCSC Ensembl
Innerchr3:154891485..154899174hg18UCSC Ensembl
Innerchr3:154891493..154899182hg17UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg387690
hg197690
hg187690
hg177690
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521905
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694677
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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