A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165560



Internal ID21511738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:132044702..132044702hg38UCSC Ensembl
chrX:131178730..131178730hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5620958
Supporting Variants
SamplesNA24385
Known GenesMST4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165560
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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