A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167357



Internal ID21480550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3823169..3861584hg38UCSC Ensembl
chrX:3741210..3779625hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3838416
hg1938416
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666520
Supporting Variants
SamplesHG03683
Known GenesLOC389906
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167357
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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