A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001956



Internal ID18744487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:896559..1236660hg38UCSC Ensembl
Innerchr3:938242..1278344hg19UCSC Ensembl
Innerchr3:913242..1253344hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38340102
hg19340103
hg18340103
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3590288
Samples
Known GenesCNTN6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001956
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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