A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17645946



Internal ID21837993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:43771635..43771635hg38UCSC Ensembl
chrX:43630882..43630882hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38684
hg19684
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6048277
Supporting Variants
Samples
Known GenesMAOB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17645946
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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