A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17645003



Internal ID21837050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:134396794..134397831hg38UCSC Ensembl
chrX:133530824..133531861hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg381038
hg191038
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6112459
Supporting Variants
Samples
Known GenesPHF6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17645003
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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