A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3001138



Internal ID16947404
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 StatusS
Merged Variantsnsv956050
Supporting Variants
SamplesBILGI_BIOE
Known GenesMTMR7
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3001138
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer