A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024782



Internal ID18767313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:169165311..169224111hg38UCSC Ensembl
Innerchr6:169565406..169624206hg19UCSC Ensembl
Innerchr6:169307331..169366131hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3858801
hg1958801
hg1858801
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3749717
Samples
Known GenesTHBS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024782
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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