A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881941



Internal ID22656917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:134373466..134377569hg38UCSC Ensembl
chrX:133507496..133511599hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg384104
hg194104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17441672
Samples
Known GenesPHF6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881941
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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