A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3981233



Internal ID19205617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:35226697..35227097hg38UCSC Ensembl
Outerchr20:33814500..33814900hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1136327
Supporting Variants
SamplesKWS1
Known GenesMMP24
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3981233
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