A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969820



Internal ID22744755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:72682302..72701844hg38UCSC Ensembl
chrX:71902152..71921694hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg3819543
hg1919543
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516701
Samples
Known GenesPHKA1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969820
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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