A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699908



Internal ID15089874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:15675093..15835341hg38UCSC Ensembl
Innerchr1:16001588..16161836hg19UCSC Ensembl
Innerchr1:15874175..16034423hg18UCSC Ensembl
Innerchr1:15746894..15907142hg17UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38160249
hg19160249
hg18160249
hg17160249
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524044
Supporting Variants
Samples
Known GenesFBLIM1, FLJ37453, PLEKHM2, SLC25A34, TMEM82, UQCRHL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699908
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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