A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150651



Internal ID15532556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:48208219..48239130hg38UCSC Ensembl
Innerchr19:48711476..48742387hg19UCSC Ensembl
Innerchr19:53403288..53434199hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3830912
hg1930912
hg1830912
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579902
Supporting Variants
SamplesHGDP01332
Known GenesCARD8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150651
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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