A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545632



Internal ID15986355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16021917..16050336hg38UCSC Ensembl
Innerchr1:16348412..16376831hg19UCSC Ensembl
Innerchr1:16220999..16249418hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3828420
hg1928420
hg1828420
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv156n54
Supporting Variantsnssv1173783
SamplesHGDP00941
Known GenesCLCNKA, CLCNKB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545632
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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