A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016665



Internal ID21926008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73914920..73916920hg38UCSC Ensembl
chr7:73329250..73331250hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg382001
hg192001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563409
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016665
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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