A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515409



Internal ID22573370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:134381381..134387880hg38UCSC Ensembl
chrX:133515411..133521910hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg386500
hg196500
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5976071
Supporting Variants
Samples
Known GenesPHF6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515409
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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