A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3939562



Internal ID21359631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:1668896..1669192hg38UCSC Ensembl
chrX:1787789..1788085hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15200170
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3939562
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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