A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6017969



Internal ID21927312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77509080..77509158hg38UCSC Ensembl
chr7:77138397..77138475hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574654
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6017969
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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