A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17648660



Internal ID21840707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:119208277..119208277hg38UCSC Ensembl
chrX:118342240..118342240hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6050115
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17648660
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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