A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661794



Internal ID15398446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3915413..3978411hg38UCSC Ensembl
Innerchr4:3917140..3980138hg19UCSC Ensembl
Innerchr4:3968061..4031034hg18UCSC Ensembl
Innerchr4:4035232..4098205hg17UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg3862999
hg1962999
hg1862974
hg1762974
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)nssv661794
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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