A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17022986



Internal ID83024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:39472000..39490000hg38UCSC Ensembl
chr9:41617018..41635018hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3818001
hg1918001
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5420604
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17022986
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.5


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