A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886947



Internal ID22661936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:127811043..127941688hg38UCSC Ensembl
chrX:126945022..127075667hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38130646
hg19130646
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446749
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886947
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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