A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545588



Internal ID16332997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:14580718..14655424hg38UCSC Ensembl
Innerchr1:14907214..14981920hg19UCSC Ensembl
Innerchr1:14779801..14854507hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3874707
hg1974707
hg1874707
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1173770
SamplesHGDP00554
Known GenesKAZN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545588
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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