A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737871



Internal ID161537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:148115606..148121800hg38UCSC Ensembl
chrX:147197126..147203320hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg386195
hg196195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138170
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737871
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00313808


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