A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3743098



Internal ID19041379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:130041790..130091985hg38UCSC Ensembl
Innerchr4:130962945..131013140hg19UCSC Ensembl
Innerchr4:131182395..131232590hg18UCSC Ensembl
Cytoband4q28.2
Allele length
AssemblyAllele length
hg3850196
hg1950196
hg1850196
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019114
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3743098
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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