A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17164865



Internal ID21460800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:107352607..107352607hg38UCSC Ensembl
chrX:106595837..106595837hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5614416
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17164865
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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