A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877552



Internal ID22652517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:134413657..134413821hg38UCSC Ensembl
chrX:133547687..133547851hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17443262
Samples
Known GenesPHF6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877552
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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