A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150652



Internal ID15529087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:48243424..48258167hg38UCSC Ensembl
Innerchr19:48746681..48761424hg19UCSC Ensembl
Innerchr19:53438493..53453236hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3814744
hg1914744
hg1814744
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579903
Supporting Variants
SamplesHGDP00734
Known GenesCARD8, LOC100505812
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150652
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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