A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545631



Internal ID15986354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16021917..16047835hg38UCSC Ensembl
Innerchr1:16348412..16374330hg19UCSC Ensembl
Innerchr1:16220999..16246917hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3825919
hg1925919
hg1825919
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv156n54
Supporting Variantsnssv1173782
SamplesHGDP00934
Known GenesCLCNKA, CLCNKB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545631
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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