A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv894847



Internal ID15842117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14620874..14623149hg38UCSC Ensembl
Innerchr19:14731686..14733961hg19UCSC Ensembl
Innerchr19:14592686..14594961hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg382276
hg192276
hg182276
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578666
Supporting Variants
Samples
Known GenesEMR3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv894847
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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