A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6261179



Internal ID22065789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23264096..23264096hg38UCSC Ensembl
chr7:23303715..23303715hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17860220
Samples
Known GenesGPNMB
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6261179
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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