A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883744



Internal ID22658726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:53969582..53971886hg38UCSC Ensembl
chrX:53996015..53998319hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg382305
hg192305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467142
Samples
Known GenesPHF8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883744
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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