A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702632



Internal ID15092598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21733..2305176hg38UCSC Ensembl
Innerchr3:63411..2346860hg19UCSC Ensembl
Innerchr3:38411..2321860hg18UCSC Ensembl
Innerchr3:38411..2321860hg17UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg382283444
hg192283450
hg182283450
hg172283450
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526340
Supporting Variants
Samples
Known GenesCHL1, CNTN4, CNTN4-AS2, CNTN6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702632
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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