A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695612



Internal ID15085578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:93026341..93035164hg38UCSC Ensembl
Innerchr9:95788623..95797446hg19UCSC Ensembl
Innerchr9:94828444..94837267hg18UCSC Ensembl
Innerchr9:92868178..92877001hg17UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg388824
hg198824
hg188824
hg178824
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521136
Supporting Variants
Samples
Known GenesFGD3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695612
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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