A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615173



Internal ID16402582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:110525275..110551223hg38UCSC Ensembl
Innerchr9:113287555..113313503hg19UCSC Ensembl
Innerchr9:112327376..112353324hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3825949
hg1925949
hg1825949
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176117
SamplesNINDS_159
Known GenesSVEP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615173
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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