A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426444



Internal ID21083997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:9338925..9346753hg38UCSC Ensembl
chr9:9338925..9346753hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg387829
hg197829
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184363
Samples
Known GenesPTPRD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426444
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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