A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv709461



Internal ID16003417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:7497092..7507352hg38UCSC Ensembl
Innerchr1:7557152..7567412hg19UCSC Ensembl
Innerchr1:7479739..7489999hg18UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3810261
hg1910261
hg1810261
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545300
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)nssv709461
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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