A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3947932



Internal ID21368001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:26194092..26194218hg38UCSC Ensembl
chrX:26212209..26212335hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15200638
SamplesHG002
Known GenesMAGEB6
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3947932
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer