A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5427992



Internal ID206875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:137103946..137124090hg38UCSC Ensembl
chrX:136186105..136206249hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3820145
hg1920145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742568
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5427992
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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