A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101728



Internal ID22010961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:150684704..150695497hg38UCSC Ensembl
chrX:149853177..149863970hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3810794
hg1910794
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645270
Samples
Known GenesMTMR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101728
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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