A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126257



Internal ID19260403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:45990435..45999922hg38UCSC Ensembl
Outerchr10:51595900..51605400hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg389488
hg199501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3984490
SamplesKWS1
Known GenesTIMM23
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126257
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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