A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17456059



Internal ID22513936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:54920945..54921187hg38UCSC Ensembl
chrX:54947378..54947620hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg38243
hg19243
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5871275
Supporting Variants
Samples
Known GenesTRO
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17456059
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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