A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3956592



Internal ID19208499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:49917486..49917543hg38UCSC Ensembl
Outerchr3:49954919..49954976hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1116988
Supporting Variants
SamplesKWS1
Known GenesMON1A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3956592
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