A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885832



Internal ID22660818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:27690351..27726938hg38UCSC Ensembl
chrX:27708468..27745055hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3836588
hg1936588
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456632
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885832
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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