A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv677878



Internal ID15414530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3915413..4081209hg38UCSC Ensembl
Innerchr4:3917140..4082936hg19UCSC Ensembl
Innerchr4:3968061..4133837hg18UCSC Ensembl
Innerchr4:4035232..4201008hg17UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38165797
hg19165797
hg18165777
hg17165777
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517008
Supporting Variants
Samples
Known GenesFAM86EP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv677878
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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