A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578160



Internal ID16365569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:583418..588305hg38UCSC Ensembl
Innerchr19:583418..588305hg19UCSC Ensembl
Innerchr19:534418..539305hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg384888
hg194888
hg184888
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv891230
Samples
Known GenesBSG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578160
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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