A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv896912



Internal ID16190868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:23489124..23878342hg38UCSC Ensembl
Innerchr19:23671926..24061144hg19UCSC Ensembl
Innerchr19:23463766..23852984hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38389219
hg19389219
hg18389219
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579049
Supporting Variants
Samples
Known GenesRPSAP58, ZNF675, ZNF681
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv896912
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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