A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv893201



Internal ID15840471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:6958123..6978002hg38UCSC Ensembl
Innerchr19:6958134..6978013hg19UCSC Ensembl
Innerchr19:6909134..6929013hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3819880
hg1919880
hg1819880
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578477
Supporting Variants
Samples
Known GenesEMR4P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv893201
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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