A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999459



Internal ID18812309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:230573..288287hg38UCSC Ensembl
Innerchr3:272256..329970hg19UCSC Ensembl
Innerchr3:247256..304970hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3857715
hg1957715
hg1857715
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3590270
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)nsv999459
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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