A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022180



Internal ID19111398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:137579612..137644463hg38UCSC Ensembl
Innerchr6:137900749..137965600hg19UCSC Ensembl
Innerchr6:137942442..138007293hg18UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3864852
hg1964852
hg1864852
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6152n100
Supporting Variantsnssv3654416
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)nsv1022180
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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