A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6257598



Internal ID22062208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34986102..34986102hg38UCSC Ensembl
chr9:34986099..34986099hg19UCSC Ensembl
Cytoband9p13.3
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 Variantsnssv17841153
Samples
Known GenesLOC101926900
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6257598
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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