A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150139



Internal ID15877115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:51722514..51856730hg38UCSC Ensembl
Innerchr19:52225767..52359983hg19UCSC Ensembl
Innerchr19:56917579..57051795hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg38134217
hg19134217
hg18134217
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579997
Supporting Variants
SamplesHGDP00936
Known GenesFPR1, FPR2, FPR3, HAS1, ZNF577
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150139
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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