A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6261202



Internal ID22065812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:25122776..25122776hg38UCSC Ensembl
chr7:25162395..25162395hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38255
hg19255
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17859943
Samples
Known GenesCYCS
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6261202
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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