A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17646121



Internal ID21838168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:73878457..73878457hg38UCSC Ensembl
chrX:73098292..73098292hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6046512
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17646121
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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