A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960211



Internal ID19204079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:66651794..66683694hg38UCSC Ensembl
Outerchr9:65989200..66021100hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3831901
hg1931901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110557
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960211
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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