A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696505



Internal ID15086471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:188144780..188171749hg38UCSC Ensembl
Innerchr4:189065934..189092903hg19UCSC Ensembl
Innerchr4:189302928..189329897hg18UCSC Ensembl
Innerchr4:189441083..189468052hg17UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg3826970
hg1926970
hg1826970
hg1726970
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519300
Supporting Variants
Samples
Known GenesTRIML1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696505
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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