A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv684303



Internal ID15074269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:15719241..15719997hg38UCSC Ensembl
Innerchr5:15719350..15720106hg19UCSC Ensembl
Innerchr5:15772350..15773106hg18UCSC Ensembl
Innerchr5:15772350..15773106hg17UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38757
hg19757
hg18757
hg17757
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516929
Supporting Variants
Samples
Known GenesFBXL7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv684303
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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