A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448075



Internal ID21105628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96399649..96405153hg38UCSC Ensembl
chr9:99161931..99167435hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg385505
hg195505
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196857
Samples
Known GenesZNF367
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448075
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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