A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017325



Internal ID19106542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:127487215..127588121hg38UCSC Ensembl
Innerchr4:128408370..128509276hg19UCSC Ensembl
Innerchr4:128627820..128728726hg18UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg38100907
hg19100907
hg18100907
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5384n100
Supporting Variantsnssv3639428, nssv3639429
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)nsv1017325
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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