A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999669



Internal ID18812519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:29013..66815hg38UCSC Ensembl
Innerchr4:29013..66707hg19UCSC Ensembl
Innerchr4:19013..56707hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3837803
hg1937695
hg1837695
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5062n100
Supporting Variantsnssv3615251, nssv3738060
Samples
Known GenesZNF595, ZNF718
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999669
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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