A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6047973



Internal ID21957206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:21858888..21858888hg38UCSC Ensembl
chrX:21877006..21877006hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg38283
hg19283
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637999
Samples
Known GenesMBTPS2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6047973
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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