A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438928



Internal ID21096481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113416601..113417235hg38UCSC Ensembl
chr9:116178881..116179515hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38635
hg19635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18174396
Samples
Known GenesC9orf43
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438928
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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