A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011872



Internal ID18754407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2782874..3057776hg38UCSC Ensembl
Innerchr3:2824558..3099460hg19UCSC Ensembl
Innerchr3:2799558..3074460hg18UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg38274903
hg19274903
hg18274903
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3590377
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)nsv1011872
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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