A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766090



Internal ID18961693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:101346042..101349443hg38UCSC Ensembl
chr4:102267199..102270600hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg383402
hg193402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073361
Supporting Variants
SamplesKWP1
Known GenesFLJ20021, PPP3CA
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766090
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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