A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17168004



Internal ID21430668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:45434811..45434871hg38UCSC Ensembl
chrX:45294056..45294116hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5667186
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17168004
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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