A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886787



Internal ID22661776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:73974298..73976813hg38UCSC Ensembl
chrX:73194133..73196648hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg382516
hg192516
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467763
Samples
Known GenesJPX
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886787
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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