A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17168632



Internal ID21455833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:75948124..75948124hg38UCSC Ensembl
chrX:75167959..75167959hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5609021
Supporting Variants
SamplesHG02492
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17168632
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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