A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884526



Internal ID22659509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:21856277..21856333hg38UCSC Ensembl
chrX:21874395..21874451hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463134
Samples
Known GenesMBTPS2, YY2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884526
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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