A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17516256



Internal ID22574218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:43948881..43965684hg38UCSC Ensembl
chrX:43808127..43824930hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3816804
hg1916804
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5976000
Supporting Variants
Samples
Known GenesNDP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17516256
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