A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3988336



Internal ID19219058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:19136862..19155734hg38UCSC Ensembl
Outerchr6:19137093..19155965hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3818873
hg1918873
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1133372
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3988336
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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