A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv891228



Internal ID16185184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:580575..582092hg38UCSC Ensembl
Innerchr19:580575..582092hg19UCSC Ensembl
Innerchr19:531575..533092hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381518
hg191518
hg181518
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578158
Supporting Variants
Samples
Known GenesBSG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv891228
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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