A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561630



Internal ID334601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:51422942..51422992hg38UCSC Ensembl
chrX:51165794..51165844hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg384776
hg194776
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736948
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561630
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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