A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6250941



Internal ID22055551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62653751..62653751hg38UCSC Ensembl
chr17:60731112..60731112hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17848921
Samples
Known GenesMRC2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6250941
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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