A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15200356



Internal ID21339171
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 StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3938564
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15200356
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