A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5600568



Internal ID21549209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95503732..95504060hg38UCSC Ensembl
chr9:98266014..98266342hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17163152
SamplesNA19238
Known GenesPTCH1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5600568
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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