A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011386



Internal ID18753920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:1987145..2359283hg38UCSC Ensembl
Innerchr3:2028829..2400967hg19UCSC Ensembl
Innerchr3:2003829..2375967hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38372139
hg19372139
hg18372139
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3739541
Samples
Known GenesCNTN4, CNTN4-AS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011386
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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