A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899772



Internal ID16193728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42889774..43209931hg38UCSC Ensembl
Innerchr19:43393926..43714083hg19UCSC Ensembl
Innerchr19:48085766..48405923hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38320158
hg19320158
hg18320158
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579734
Supporting Variants
Samples
Known GenesPSG11, PSG2, PSG4, PSG5, PSG6, PSG7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899772
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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