A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956124



Internal ID16958311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:51858145..51858266hg38UCSC Ensembl
Outerchr10:53617905..53618026hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3004889
SamplesBILGI_BIOE
Known GenesPRKG1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956124
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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