A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv898771



Internal ID15846041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35268140..35270013hg38UCSC Ensembl
Innerchr19:35759043..35760916hg19UCSC Ensembl
Innerchr19:40450883..40452756hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg381874
hg191874
hg181874
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579391
Supporting Variants
Samples
Known GenesUSF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv898771
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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