A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013825



Internal ID18756357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:256421..312812hg38UCSC Ensembl
Innerchr3:298104..354495hg19UCSC Ensembl
Innerchr3:273104..329495hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3856392
hg1956392
hg1856392
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3590275, nssv3590274
Samples
Known GenesCHL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013825
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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