A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436717



Internal ID21094270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129692226..129761076hg38UCSC Ensembl
chr9:132454505..132523355hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3868851
hg1968851
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18174647
Samples
Known GenesPRRX2, PTGES
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436717
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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