A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1116644



Internal ID19280004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:42097572..42104802hg38UCSC Ensembl
Outerchr10:42596699..42600250hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg387231
hg193552
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv426n106
Supporting Variantsnssv3979208
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1116644
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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