A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515345



Internal ID22573306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:129740288..129748750hg38UCSC Ensembl
chrX:128874264..128882726hg19UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg388463
hg198463
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5971646
Supporting Variants
Samples
Known GenesXPNPEP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515345
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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