A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959199



Internal ID19205631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:121143046..121156858hg38UCSC Ensembl
Outerchr8:122155286..122169098hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg3813813
hg1913813
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1109986
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959199
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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