A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882849



Internal ID22657826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:121546374..121548362hg38UCSC Ensembl
chrX:120680228..120682216hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg381989
hg191989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17447088
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882849
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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