A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1112392



Internal ID18934888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:86100..373360hg38UCSC Ensembl
Outerchr4:85991..367149hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38287261
hg19281159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2697n106
Supporting Variantsnssv3966472
SamplesKWS2
Known GenesZNF141, ZNF595, ZNF718, ZNF732, ZNF876P
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1112392
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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