A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6261161



Internal ID22065771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:21584961..21584961hg38UCSC Ensembl
chr7:21624579..21624579hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17860203
Samples
Known GenesDNAH11
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6261161
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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