A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057365



Internal ID19146584
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 StatusM
Merged Variantsdgv3124n100
Supporting Variantsnssv3720025, nssv3560959
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)nsv1057365
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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