A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703507



Internal ID15093473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:74213719..74397605hg38UCSC Ensembl
Innerchr17:72209858..72393744hg19UCSC Ensembl
Innerchr17:69721453..69905339hg18UCSC Ensembl
Innerchr17:69721453..69905339hg17UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38183887
hg19183887
hg18183887
hg17183887
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517569
Supporting Variants
Samples
Known GenesBTBD17, DNAI2, GPR142, KIF19, TTYH2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703507
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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