A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165192



Internal ID21460876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:104363892..104365881hg38UCSC Ensembl
chrX:103608573..103610562hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg381990
hg191990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666099
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165192
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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