A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545160



Internal ID15985883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:4690970..4727059hg38UCSC Ensembl
Innerchr1:4751030..4787119hg19UCSC Ensembl
Innerchr1:4650890..4686979hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3836090
hg1936090
hg1836090
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1173647
SamplesNINDS_66
Known GenesAJAP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545160
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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