A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165076



Internal ID21467260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:119332397..119332515hg38UCSC Ensembl
chrX:118466360..118466478hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665038
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165076
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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