A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17638961



Internal ID21831008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:89319465..89319465hg38UCSC Ensembl
chrX:88574464..88574464hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6050324
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17638961
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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