A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3928817



Internal ID21348887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:141906140..141906245hg38UCSC Ensembl
chrX:140993926..140994031hg19UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15200268
SamplesHG002
Known GenesMAGEC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3928817
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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