A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv892046



Internal ID16186002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1950722..1952091hg38UCSC Ensembl
Innerchr19:1950721..1952090hg19UCSC Ensembl
Innerchr19:1901721..1903090hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381370
hg191370
hg181370
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578365
Supporting Variants
Samples
Known GenesCSNK1G2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv892046
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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