A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165802



Internal ID21445479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:139963637..139963769hg38UCSC Ensembl
chrX:139045796..139045928hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666745
Supporting Variants
SamplesHG00732
Known GenesCXorf66
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165802
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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