A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv709153



Internal ID15656423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:6262876..6289815hg38UCSC Ensembl
Innerchr1:6322936..6349875hg19UCSC Ensembl
Innerchr1:6245523..6272462hg18UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg3826940
hg1926940
hg1826940
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545239
Supporting Variants
Samples
Known GenesACOT7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv709153
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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