A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17516375



Internal ID22574338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:54036583..54045356hg38UCSC Ensembl
chrX:54063016..54071789hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg388774
hg198774
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5975908
Supporting Variants
Samples
Known GenesPHF8
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17516375
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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