A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17160575



Internal ID21427857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135847949..135847949hg38UCSC Ensembl
chr9:138739795..138739795hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38219
hg19219
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5630700
Supporting Variants
SamplesHG00731
Known GenesCAMSAP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17160575
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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