A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140229



Internal ID339422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:12868756..12875875hg38UCSC Ensembl
chr3:12910255..12917374hg19UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg387120
hg197120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16930930
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140229
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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