A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137934



Internal ID19272022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:68520070..68520148hg38UCSC Ensembl
Outerchr10:70279827..70279905hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3990455
SamplesKWS2
Known GenesSLC25A16
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137934
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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