A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3982099



Internal ID19222229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:1303630..1303691hg38UCSC Ensembl
Outerchr1:1239010..1239071hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1119655
Supporting Variants
SamplesKWS1
Known GenesACAP3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3982099
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