A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6257624



Internal ID22062234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:37688274..37688274hg38UCSC Ensembl
chr9:37688271..37688271hg19UCSC Ensembl
Cytoband9p13.2
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 Variantsnssv17841177
Samples
Known GenesFRMPD1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6257624
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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