A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv956050



Internal ID16958237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:17408105..17408407hg38UCSC Ensembl
Outerchr8:17265614..17265916hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001138
SamplesBILGI_BIOE
Known GenesMTMR7
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv956050
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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