A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3983973



Internal ID19227950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:9086726..9086805hg38UCSC Ensembl
Outerchr3:9128410..9128489hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1125769
Supporting Variants
SamplesKWS2
Known GenesSRGAP3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3983973
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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