A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3934945



Internal ID21355014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:151915682..151917726hg38UCSC Ensembl
chrX:151084154..151086198hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg382045
hg192045
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15200432
SamplesHG002
Known GenesMAGEA4
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3934945
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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