A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975977



Internal ID22750912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:134423843..134429592hg38UCSC Ensembl
chrX:133557873..133563622hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg385750
hg195750
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515412
Samples
Known GenesPHF6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975977
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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