A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1121457



Internal ID19282384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:41693522..41856364hg38UCSC Ensembl
Outerchr10:42383845..42600108hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38162843
hg19216264
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv418n106
Supporting Variantsnssv3965458
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1121457
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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