A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698932



Internal ID15088898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:15723524..15735847hg38UCSC Ensembl
Innerchr5:15723633..15735956hg19UCSC Ensembl
Innerchr5:15776633..15788956hg18UCSC Ensembl
Innerchr5:15776633..15788956hg17UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3812324
hg1912324
hg1812324
hg1712324
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)nssv698932
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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