A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871275



Internal ID22646212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:54920945..54921187hg38UCSC Ensembl
chrX:54947378..54947620hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg38243
hg19243
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456059
Samples
Known GenesTRO
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871275
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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