A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705809



Internal ID15442461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:78291626..78301191hg38UCSC Ensembl
Innerchr17:76287707..76297272hg19UCSC Ensembl
Innerchr17:73799302..73808867hg18UCSC Ensembl
Innerchr17:73799302..73808867hg17UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg389566
hg199566
hg189566
hg179566
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516327
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705809
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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