A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5887197



Internal ID22662189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:133524157..133529258hg38UCSC Ensembl
chrX:132658185..132663286hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg385102
hg195102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436917
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5887197
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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