A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579077



Internal ID16366486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:23901617..24307497hg38UCSC Ensembl
Innerchr19:24084419..24490299hg19UCSC Ensembl
Innerchr19:23876259..24282139hg18UCSC Ensembl
Cytoband19p11
Allele length
AssemblyAllele length
hg38405881
hg19405881
hg18405881
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv896966
Samples
Known GenesHAVCR1P1, ZNF254, ZNF726
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579077
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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