A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141425



Internal ID340621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99901032..99902986hg38UCSC Ensembl
chr9:102663314..102665268hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg381955
hg191955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025530
Samples
Known GenesLOC441461
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141425
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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