A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899936



Internal ID15847206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:45356868..45365051hg38UCSC Ensembl
Innerchr19:45860126..45868309hg19UCSC Ensembl
Innerchr19:50551966..50560149hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg388184
hg198184
hg188184
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579869
Supporting Variants
Samples
Known GenesERCC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899936
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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