A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6065272



Internal ID21974505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:82462994..82462994hg38UCSC Ensembl
chr7:82092310..82092310hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38208
hg19208
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565734
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6065272
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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