A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025531



Internal ID84754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99903490..99903540hg38UCSC Ensembl
chr9:102665772..102665822hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5542944
Supporting Variants
Samples
Known GenesLOC441461
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025531
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002498


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