A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142208



Internal ID341408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28507144..28507456hg38UCSC Ensembl
chr10:28796073..28796385hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17033415
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142208
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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