A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3970870



Internal ID19227447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:101592036..101592107hg38UCSC Ensembl
Outerchr11:101462767..101462838hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1122661
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3970870
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