A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3763533



Internal ID18964954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:86088..373354hg38UCSC Ensembl
chr4:85979..367143hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38287267
hg19281165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1074123
Supporting Variants
SamplesKWP1
Known GenesZNF141, ZNF595, ZNF718, ZNF732, ZNF876P
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3763533
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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