A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv678986



Internal ID15068952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:10132020..10133530hg38UCSC Ensembl
Innerchr17:10035337..10036847hg19UCSC Ensembl
Innerchr17:9976062..9977572hg18UCSC Ensembl
Innerchr17:9976062..9977572hg17UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg381511
hg191511
hg181511
hg171511
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520771
Supporting Variants
Samples
Known GenesGAS7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv678986
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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