A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3977856



Internal ID19245234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:63864266..63918366hg38UCSC Ensembl
Outerchr9:68460000..68514100hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3854101
hg1954101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1125050
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3977856
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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