A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007298



Internal ID18749829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:1829591..2292967hg38UCSC Ensembl
Innerchr3:1871275..2334651hg19UCSC Ensembl
Innerchr3:1846275..2309651hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38463377
hg19463377
hg18463377
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3590343, nssv3590344
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)nsv1007298
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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