A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6261162



Internal ID22065772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:21608071..21608071hg38UCSC Ensembl
chr7:21647689..21647689hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17860204
Samples
Known GenesDNAH11
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6261162
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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