A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6434110



Internal ID21091663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:6457283..6457519hg38UCSC Ensembl
chr8:6314804..6315040hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38237
hg19237
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169458
Samples
Known GenesMCPH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6434110
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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