A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765936



Internal ID19310979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:152088463..152093020hg38UCSC Ensembl
chr4:153009615..153014172hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg384558
hg194558
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1074763
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765936
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer