A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1113256



Internal ID18913059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:15098649..15098711hg38UCSC Ensembl
Outerchr10:15140648..15140710hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3968163
SamplesKWS2
Known GenesRPP38
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1113256
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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