A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001161



Internal ID21910504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:91948381..91953764hg38UCSC Ensembl
chr8:92960609..92965992hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg385384
hg195384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17579350
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001161
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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