A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167994



Internal ID21463071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:45155027..45155161hg38UCSC Ensembl
chrX:45014272..45014406hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666973
Supporting Variants
SamplesHG03009
Known GenesCXorf36
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167994
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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