A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv544987



Internal ID15985710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1342153..1350850hg38UCSC Ensembl
Innerchr1:1277533..1286230hg19UCSC Ensembl
Innerchr1:1267396..1276093hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg388698
hg198698
hg188698
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv29n54
Supporting Variantsnssv708554
Samples
Known GenesDVL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv544987
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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