A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665095



Internal ID15055061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:30485102..30598335hg38UCSC Ensembl
Innerchr17:28812120..28925353hg19UCSC Ensembl
Innerchr17:25836246..25949479hg18UCSC Ensembl
Innerchr17:25836246..25949479hg17UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38113234
hg19113234
hg18113234
hg17113234
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515870
Supporting Variants
Samples
Known GenesGOSR1, LRRC37BP1, TBC1D29
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665095
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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