A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17168427



Internal ID21466247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:72178792..72178987hg38UCSC Ensembl
chrX:71398642..71398837hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5664546
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17168427
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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