A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026638



Internal ID18769170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:24347744..24475072hg38UCSC Ensembl
Innerchr6:24347972..24475300hg19UCSC Ensembl
Innerchr6:24455951..24583279hg18UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg38127329
hg19127329
hg18127329
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654838
Samples
Known GenesDCDC2, GPLD1, KAAG1, MRS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026638
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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