A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024830



Internal ID18767361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167194096..167396465hg38UCSC Ensembl
Innerchr6:167607584..167809953hg19UCSC Ensembl
Innerchr6:167527574..167729943hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38202370
hg19202370
hg18202370
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6196n100
Supporting Variantsnssv3655406
Samples
Known GenesTCP10, TTLL2, UNC93A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024830
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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