A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6259565



Internal ID22064175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:83278986..83278986hg38UCSC Ensembl
chrX:82533994..82533994hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38220
hg19220
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17851614
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6259565
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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