A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682203



Internal ID15072169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:136388707..136581890hg38UCSC Ensembl
Innerchr3:136107549..136300732hg19UCSC Ensembl
Innerchr3:137590239..137783422hg18UCSC Ensembl
Innerchr3:137590247..137783430hg17UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg38193184
hg19193184
hg18193184
hg17193184
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520012
Supporting Variants
Samples
Known GenesSTAG1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv682203
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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