A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142526



Internal ID341726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:142588360..142795710hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38207351
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv491n206
Supporting Variantsnssv17006365
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142526
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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