A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3956826



Internal ID19205245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:5416949..5417014hg38UCSC Ensembl
Outerchr5:5417062..5417127hg19UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1114644
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3956826
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