A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141981



Internal ID341181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:92914014..92925801hg38UCSC Ensembl
chr7:92543328..92555115hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg3811788
hg1911788
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16999087
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141981
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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