A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427503



Internal ID21085056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:97718655..97739320hg38UCSC Ensembl
chr8:98730883..98751548hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3820666
hg1920666
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173554
Samples
Known GenesMTDH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427503
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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