A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028537



Internal ID19117755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167199775..167247175hg38UCSC Ensembl
Innerchr6:167613263..167660663hg19UCSC Ensembl
Innerchr6:167533253..167580653hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3847401
hg1947401
hg1847401
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6195n100
Supporting Variantsnssv3655412, nssv3655413
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)nsv1028537
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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