A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762440



Internal ID19306818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:68525481..68591182hg38UCSC Ensembl
chr4:69391199..69456900hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3865702
hg1965702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1074723
Supporting Variants
SamplesKWP1
Known GenesUGT2B17
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762440
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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