A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3994042



Internal ID18885938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:77915319..77915445hg38UCSC Ensembl
Outerchr9:80530235..80530361hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1143227
Supporting Variants
SamplesKWS2
Known GenesGNAQ
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3994042
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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