A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578949



Internal ID16366358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:21007766..21061243hg38UCSC Ensembl
Innerchr19:21190572..21244049hg19UCSC Ensembl
Innerchr19:20982412..21035889hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg3853478
hg1953478
hg1853478
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv896578
Samples
Known GenesZNF430
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578949
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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