A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3957517



Internal ID18873967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:93335582..93335671hg38UCSC Ensembl
Outerchr10:95095339..95095428hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1128081
Supporting Variants
SamplesKWS1
Known GenesMYOF
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3957517
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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