A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv890989



Internal ID16184945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:404543..411003hg38UCSC Ensembl
Innerchr19:404543..411003hg19UCSC Ensembl
Innerchr19:355543..362003hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg386461
hg196461
hg186461
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578087
Supporting Variants
Samples
Known GenesC2CD4C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv890989
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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