A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3938564



Internal ID21358634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:28076754..28076812hg38UCSC Ensembl
chrX:28094871..28094929hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15200356
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3938564
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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