A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17642529



Internal ID21834576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:49181565..49181565hg38UCSC Ensembl
chrX:49037915..49037915hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6051913
Supporting Variants
Samples
Known GenesPRICKLE3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17642529
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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