A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv957350



Internal ID16959537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:12734340..12734421hg38UCSC Ensembl
Outerchr10:12776339..12776420hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3004910
SamplesBILGI_BIOE
Known GenesCAMK1D
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv957350
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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