A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454106



Internal ID21111659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:70146701..70150100hg38UCSC Ensembl
chr9:72761617..72765016hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg383400
hg193400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193444
Samples
Known GenesMAMDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6454106
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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