A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010537



Internal ID21919880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77508825..77508940hg38UCSC Ensembl
chr7:77138142..77138257hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565647
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010537
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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