A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3981369



Internal ID18871189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:85613594..85614494hg38UCSC Ensembl
Outerchr16:85647200..85648100hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1144777
Supporting Variants
SamplesKWS1
Known GenesGSE1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3981369
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