A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17639374



Internal ID21831421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:137315110..137315110hg38UCSC Ensembl
chrX:136397269..136397269hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg381142
hg191142
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6042101
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17639374
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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