A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv690552



Internal ID15427204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:153350014..153356087hg38UCSC Ensembl
Innerchr3:153067803..153073876hg19UCSC Ensembl
Innerchr3:154550493..154556566hg18UCSC Ensembl
Innerchr3:154550501..154556574hg17UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg386074
hg196074
hg186074
hg176074
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520682
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv690552
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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