A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515212



Internal ID22573171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:11713313..11716946hg38UCSC Ensembl
chrX:11731433..11735066hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg383634
hg193634
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5976110
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515212
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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