A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899260



Internal ID15846530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:39514000..39642798hg38UCSC Ensembl
Innerchr19:40004640..40133438hg19UCSC Ensembl
Innerchr19:44696480..44825278hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38128799
hg19128799
hg18128799
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579509
Supporting Variants
Samples
Known GenesEID2, EID2B, LGALS13, LOC100129935, SELV
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899260
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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