A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545912



Internal ID15986635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:27483806..27618848hg38UCSC Ensembl
Innerchr1:27810317..27945359hg19UCSC Ensembl
Innerchr1:27682904..27817946hg18UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38135043
hg19135043
hg18135043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv219n54
Supporting Variantsnssv1173803
SamplesHGDP00861
Known GenesAHDC1, FGR, WASF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545912
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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