A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428125



Internal ID21085678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:8526542..8526978hg38UCSC Ensembl
chr9:8526542..8526978hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38437
hg19437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178182
Samples
Known GenesPTPRD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428125
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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