A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1120225



Internal ID18920566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:96920635..96920731hg38UCSC Ensembl
Outerchr10:98680392..98680488hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961004
SamplesKWS1
Known GenesLCOR
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1120225
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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