A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899621



Internal ID16193577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42776391..42857733hg38UCSC Ensembl
Innerchr19:43280543..43361885hg19UCSC Ensembl
Innerchr19:47972383..48053725hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3881343
hg1981343
hg1881343
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579645
Supporting Variants
Samples
Known GenesLOC100289650, PSG10P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899621
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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