A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3984406



Internal ID19225895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:20767288..20767545hg38UCSC Ensembl
Outerchr16:20778610..20778867hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38258
hg19258
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1126177
Supporting Variants
SamplesKWS1
Known GenesACSM3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3984406
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