A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899563



Internal ID16193519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:41896562..41897164hg38UCSC Ensembl
Innerchr19:42400635..42401313hg19UCSC Ensembl
Innerchr19:47092475..47093153hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38603
hg19679
hg18679
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579616
Supporting Variants
Samples
Known GenesARHGEF1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899563
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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