A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3970381



Internal ID18883930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:93314799..93314856hg38UCSC Ensembl
Outerchr10:95074556..95074613hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1134042
Supporting Variants
SamplesKWS2
Known GenesMYOF
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3970381
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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