A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704947



Internal ID15441599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:1330341..1365389hg38UCSC Ensembl
Innerchr17:1233635..1268683hg19UCSC Ensembl
Innerchr17:1180385..1215433hg18UCSC Ensembl
Innerchr17:1180385..1215433hg17UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3835049
hg1935049
hg1835049
hg1735049
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528360
Supporting Variants
Samples
Known GenesYWHAE
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704947
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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