A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016393



Internal ID18758928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:71180534..71232083hg38UCSC Ensembl
Innerchr6:71890237..71941786hg19UCSC Ensembl
Innerchr6:71946958..71998507hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3851550
hg1951550
hg1851550
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3658809, nssv3658810, nssv3747082
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)nsv1016393
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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