A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3771204



Internal ID18958925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:68729581..69012282hg38UCSC Ensembl
chr4:69595299..69878000hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38282702
hg19282702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1074180
Supporting Variants
SamplesKWP1
Known GenesUGT2A3, UGT2B10
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3771204
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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