A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165245



Internal ID21473802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:110048092..110048149hg38UCSC Ensembl
chrX:109291320..109291377hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5671598
Supporting Variants
SamplesHG03371
Known GenesTMEM164
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165245
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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