A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv673095



Internal ID15409747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3922001..4198033hg38UCSC Ensembl
Innerchr4:3923728..4199760hg19UCSC Ensembl
Innerchr4:3974654..4250661hg18UCSC Ensembl
Innerchr4:4041825..4317832hg17UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38276033
hg19276033
hg18276008
hg17276008
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517008
Supporting Variants
Samples
Known GenesFAM86EP, OTOP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv673095
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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