A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167848



Internal ID21510987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:5241431..5246163hg38UCSC Ensembl
chrX:5159472..5164204hg19UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg384733
hg194733
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666855
Supporting Variants
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167848
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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