A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3742886



Internal ID18694481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:91262174..91338334hg38UCSC Ensembl
Innerchr4:92183325..92259485hg19UCSC Ensembl
Innerchr4:92402348..92478508hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3876161
hg1976161
hg1876161
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013025
Supporting Variants
Samples
Known GenesCCSER1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3742886
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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