A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545131



Internal ID16332540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:3954031..4020720hg38UCSC Ensembl
Innerchr1:4014091..4080780hg19UCSC Ensembl
Innerchr1:3913951..3980640hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3866690
hg1966690
hg1866690
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1172592
SamplesHGDP00586
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545131
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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