A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704959



Internal ID15441611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:151492402..151500489hg38UCSC Ensembl
Innerchr3:151210190..151218277hg19UCSC Ensembl
Innerchr3:152692880..152700967hg18UCSC Ensembl
Innerchr3:152692888..152700975hg17UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg388088
hg198088
hg188088
hg178088
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528372
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704959
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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