A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030686



Internal ID19119905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:140808935..141427942hg38UCSC Ensembl
Innerchr6:141130072..141749079hg19UCSC Ensembl
Innerchr6:141171765..141790772hg18UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38619008
hg19619008
hg18619008
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6159n100
Supporting Variantsnssv3654444
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)nsv1030686
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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