A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1123662



Internal ID19282018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:72472897..72472956hg38UCSC Ensembl
Outerchr3:72522048..72522107hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3973129, nssv3986216
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1123662
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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