A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881137



Internal ID22656111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:134393635..134413487hg38UCSC Ensembl
chrX:133527665..133547517hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg3819853
hg1919853
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444050
Samples
Known GenesPHF6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881137
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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