A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3613358



Internal ID18911639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:9394920..9560119hg38UCSC Ensembl
Innerchr4:9396646..9561739hg19UCSC Ensembl
Innerchr4:9005744..9170837hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38165200
hg19165094
hg18165094
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001604
Supporting Variants
Samples
Known GenesDEFB131, LOC650293, MIR548I2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3613358
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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