A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107151



Internal ID22016384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:10713612..10730862hg38UCSC Ensembl
chrX:10681652..10698902hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3817251
hg1917251
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645590
Samples
Known GenesMID1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107151
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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