A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1135630



Internal ID19279003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:185520443..185522919hg38UCSC Ensembl
Outerchr4:186441597..186444073hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg382477
hg192477
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3989192
SamplesKWS2
Known GenesPDLIM3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1135630
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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