A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17516984



Internal ID22574947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:9711797..9717291hg38UCSC Ensembl
chrX:9679837..9685331hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg385495
hg195495
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5968514
Supporting Variants
Samples
Known GenesTBL1X
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17516984
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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