A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3956675



Internal ID18860513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:64621..67995hg38UCSC Ensembl
Outerchr4:64513..67887hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg383375
hg193375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1114477
Supporting Variants
SamplesKWS1
Known GenesZNF595, ZNF718
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3956675
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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