A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3941699



Internal ID21361770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:1638902..1641373hg38UCSC Ensembl
chrX:1757795..1760266hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg382472
hg192472
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15200167
SamplesHG002
Known GenesASMT
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3941699
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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