A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960229



Internal ID19217552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:68232984..68237084hg38UCSC Ensembl
Outerchr9:70847900..70852000hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg384101
hg194101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110575
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960229
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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