A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007848



Internal ID18750379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2326335..2345440hg38UCSC Ensembl
Innerchr3:2368019..2387124hg19UCSC Ensembl
Innerchr3:2343019..2362124hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3819106
hg1919106
hg1819106
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3590373
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)nsv1007848
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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