A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036295



Internal ID19125514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:43354078..43772103hg38UCSC Ensembl
Innerchr14:43823281..44241306hg19UCSC Ensembl
Innerchr14:42893031..43311056hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38418026
hg19418026
hg18418026
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1890n100
Supporting Variantsnssv3712307, nssv3530235, nssv3530234, nssv3530236, nssv3712306, nssv3530233
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)nsv1036295
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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