A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3560964



Internal ID18859245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:21432315..21642949hg38UCSC Ensembl
Innerchr17:21335627..21547725hg19UCSC Ensembl
Innerchr17:21276220..21488318hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38210635
hg19212099
hg18212099
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056663
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)nssv3560964
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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