A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6074266



Internal ID21983499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:54545953..54545953hg38UCSC Ensembl
chr7:54613646..54613646hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558217
Samples
Known GenesVSTM2A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6074266
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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