A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545911



Internal ID16333320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:27483806..27605187hg38UCSC Ensembl
Innerchr1:27810317..27931698hg19UCSC Ensembl
Innerchr1:27682904..27804285hg18UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38121382
hg19121382
hg18121382
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv219n54
Supporting Variantsnssv1173802
SamplesHGDP00850
Known GenesAHDC1, WASF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545911
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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