A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv896184



Internal ID15843454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20411600..20584511hg38UCSC Ensembl
Innerchr19:20594407..20767317hg19UCSC Ensembl
Innerchr19:20386247..20559157hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38172912
hg19172911
hg18172911
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578831
Supporting Variants
Samples
Known GenesZNF737, ZNF826P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv896184
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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