A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv897586



Internal ID15844856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:29974289..30048552hg38UCSC Ensembl
Innerchr19:30465196..30539459hg19UCSC Ensembl
Innerchr19:35157036..35231299hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3874264
hg1974264
hg1874264
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579283
Supporting Variants
Samples
Known GenesURI1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv897586
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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