A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115647



Internal ID19271808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:170879711..170884111hg38UCSC Ensembl
Outerchr3:170597500..170601900hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg384401
hg194401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3977456, nssv3987361
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115647
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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