A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024981



Internal ID19114199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:140812927..141421545hg38UCSC Ensembl
Innerchr6:141134064..141742682hg19UCSC Ensembl
Innerchr6:141175757..141784375hg18UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38608619
hg19608619
hg18608619
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6159n100
Supporting Variantsnssv3654445
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)nsv1024981
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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