A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17638395



Internal ID21830442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:150690018..150693838hg38UCSC Ensembl
chrX:149858491..149862311hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg383821
hg193821
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6110060
Supporting Variants
Samples
Known GenesMTMR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17638395
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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