A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3977132



Internal ID19240805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:26586653..26589253hg38UCSC Ensembl
Outerchr11:26608200..26610800hg19UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg382601
hg192601
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1139546
Supporting Variants
SamplesKWS2
Known GenesANO3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3977132
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer