A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515378



Internal ID22573339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:131756897..131795157hg38UCSC Ensembl
chrX:130890925..130929185hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg3838261
hg1938261
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5976870
Supporting Variants
Samples
Known GenesLOC286467
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515378
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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