A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545635



Internal ID16333044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16033992..16034386hg38UCSC Ensembl
Innerchr1:16360487..16360881hg19UCSC Ensembl
Innerchr1:16233074..16233468hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38395
hg19395
hg18395
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv710829, nssv710832, nssv710810, nssv710836, nssv710816, nssv710817, nssv710827, nssv710833, nssv710831, nssv710828, nssv710819, nssv710821, nssv710815, nssv710823, nssv710809, nssv710837, nssv710820, nssv710812, nssv710830, nssv710813, nssv710811, nssv710822, nssv710826, nssv710814, nssv710834, nssv710824, nssv710835, nssv710818, nssv710825
Samples
Known GenesCLCNKA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545635
Frequency
Sample Size17421
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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