A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17642075



Internal ID21834122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:40211102..40211102hg38UCSC Ensembl
chrX:40070355..40070355hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6046385
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17642075
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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