A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421417



Internal ID21078970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:17345649..17347525hg38UCSC Ensembl
chr8:17203158..17205034hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg381877
hg191877
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166307
Samples
Known GenesMTMR7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421417
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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