A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660184



Internal ID15050150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:126103429..126135566hg38UCSC Ensembl
Innerchr3:125822272..125854409hg19UCSC Ensembl
Innerchr3:127304962..127337099hg18UCSC Ensembl
Innerchr3:127304970..127337107hg17UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg3832138
hg1932138
hg1832138
hg1732138
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520037
Supporting Variants
Samples
Known GenesALDH1L1, ALDH1L1-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660184
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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