A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013960



Internal ID18756492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2153628..2183597hg38UCSC Ensembl
Innerchr3:2195312..2225281hg19UCSC Ensembl
Innerchr3:2170312..2200281hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3829970
hg1929970
hg1829970
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3590366
Samples
Known GenesCNTN4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013960
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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