A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545619



Internal ID15986342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:15802946..15834894hg38UCSC Ensembl
Innerchr1:16129441..16161389hg19UCSC Ensembl
Innerchr1:16002028..16033976hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3831949
hg1931949
hg1831949
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv710538
Samples
Known GenesFLJ37453, UQCRHL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545619
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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