A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663029



Internal ID15052995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:197066987..197291254hg38UCSC Ensembl
Innerchr3:196793858..197018125hg19UCSC Ensembl
Innerchr3:198278255..198502522hg18UCSC Ensembl
Innerchr3:198282168..198506435hg17UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38224268
hg19224268
hg18224268
hg17224268
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516873
Supporting Variants
Samples
Known GenesDLG1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv663029
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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