A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442209



Internal ID21099762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72057408..72058322hg38UCSC Ensembl
chr9:74672324..74673238hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38915
hg19915
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191711
Samples
Known GenesC9orf57
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442209
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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