A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3720025



Internal ID19018306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:21428918..21641965hg38UCSC Ensembl
Innerchr17:21332230..21545210hg19UCSC Ensembl
Innerchr17:21272823..21485803hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38213048
hg19212981
hg18212981
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057365
Supporting Variants
Samples
Known GenesC17orf51
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3720025
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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