A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872000



Internal ID22646938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103523967..103554101hg38UCSC Ensembl
chrX:102778895..102809029hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg3830135
hg1930135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2292n209
Supporting Variantsnssv17437313
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872000
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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