A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17649676



Internal ID21841723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:118368477..118368477hg38UCSC Ensembl
chrX:117502440..117502440hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6057519
Supporting Variants
Samples
Known GenesWDR44
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17649676
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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