A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556320



Internal ID329460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:30915115..30915166hg38UCSC Ensembl
chrX:30933232..30933283hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg38256
hg19256
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739830
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556320
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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