A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1002289



Internal ID15949559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:70815237..70911218hg38UCSC Ensembl
Innerchr4:71680954..71776935hg19UCSC Ensembl
Innerchr4:71899818..71995799hg18UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3895982
hg1995982
hg1895982
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594651
Supporting Variants
Samples
Known GenesGRSF1, MOB1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1002289
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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