A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999998



Internal ID19159534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:120600940..120622252hg38UCSC Ensembl
Innerchr4:121522095..121543407hg19UCSC Ensembl
Innerchr4:121741545..121762857hg18UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3821313
hg1921313
hg1821313
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5375n100
Supporting Variantsnssv3639355
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)nsv999998
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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