A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3641103



Internal ID18939384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:134441463..135374829hg38UCSC Ensembl
Innerchr4:135362618..136295984hg19UCSC Ensembl
Innerchr4:135582068..136515434hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38933367
hg19933367
hg18933367
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017663
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)nssv3641103
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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