A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17168270



Internal ID21507438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:72682212..72682212hg38UCSC Ensembl
chrX:71902062..71902062hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5623530
Supporting Variants
SamplesNA19983
Known GenesPHKA1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17168270
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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