A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17161742



Internal ID21412692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36474249..36475081hg38UCSC Ensembl
chr9:36474246..36475078hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38833
hg19833
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591354
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17161742
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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