A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060300



Internal ID19149519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36714591..36742497hg38UCSC Ensembl
Innerchr17:35071037..35098785hg19UCSC Ensembl
Innerchr17:32145150..32172898hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3827907
hg1927749
hg1827749
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3562540
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060300
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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