A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17649668



Internal ID21841715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:19553955..19553955hg38UCSC Ensembl
chrX:19572073..19572073hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6046854
Supporting Variants
Samples
Known GenesSH3KBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17649668
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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