A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142669



Internal ID341870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98237683..98238808hg38UCSC Ensembl
chr9:100999965..101001090hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg381126
hg191126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17026883
Samples
Known GenesTBC1D2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142669
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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