A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129502



Internal ID19251275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:113689911..113690038hg38UCSC Ensembl
Outerchr10:115449670..115449797hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3963734
SamplesKWS1
Known GenesCASP7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129502
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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