A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv709390



Internal ID16003346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:6962639..6963434hg38UCSC Ensembl
Innerchr1:7022699..7023494hg19UCSC Ensembl
Innerchr1:6945286..6946081hg18UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg38796
hg19796
hg18796
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545282
Supporting Variants
Samples
Known GenesCAMTA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv709390
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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