A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011065



Internal ID19100282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:121694409..121741169hg38UCSC Ensembl
Innerchr1:121436207..121482967hg19UCSC Ensembl
Innerchr1:121137730..121184490hg18UCSC Ensembl
Cytoband1p11.1
Allele length
AssemblyAllele length
hg3846761
hg1946761
hg1846761
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3487834, nssv3702083, nssv3501172, nssv3486265, nssv3491258, nssv3502102, nssv3702084
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)nsv1011065
Frequency
Sample Size11257
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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