A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141983



Internal ID341183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66329191..66391191hg38UCSC Ensembl
chr9:42129989..42192552hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3862001
hg1962564
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024148
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141983
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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