A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007386



Internal ID18749917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:117162537..117179558hg38UCSC Ensembl
Innerchr1:117705159..117722180hg19UCSC Ensembl
Innerchr1:117506682..117523703hg18UCSC Ensembl
Cytoband1p13.1
Allele length
AssemblyAllele length
hg3817022
hg1917022
hg1817022
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3492663
Samples
Known GenesVTCN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007386
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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