A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032647



Internal ID19121869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:78147537..78332080hg38UCSC Ensembl
Innerchr6:78857254..79041797hg19UCSC Ensembl
Innerchr6:78913973..79098516hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38184544
hg19184544
hg18184544
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6024n100
Supporting Variantsnssv3659066, nssv3659067, nssv3659068, nssv3659065, nssv3659069, nssv3659070, nssv3659071, nssv3659072
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)nsv1032647
Frequency
Sample Size11257
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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