A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6261032



Internal ID22065642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:7575916..7575916hg38UCSC Ensembl
chr7:7615547..7615547hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17859669
Samples
Known GenesMIOS
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6261032
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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