A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6241992



Internal ID22046602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42496114..42496114hg38UCSC Ensembl
chr15:42788312..42788312hg19UCSC Ensembl
Cytoband15q15.1
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 Variantsnssv17846434
Samples
Known GenesSNAP23
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6241992
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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