A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545910



Internal ID15986633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:27459823..27610945hg38UCSC Ensembl
Innerchr1:27786334..27937456hg19UCSC Ensembl
Innerchr1:27658921..27810043hg18UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38151123
hg19151123
hg18151123
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv219n54
Supporting Variantsnssv712045
Samples
Known GenesAHDC1, WASF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545910
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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