A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017663



Internal ID19106880
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 StatusM
Merged Variants
Supporting Variantsnssv3641103
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)nsv1017663
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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