A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169727



Internal ID21401247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:11298077..11298077hg38UCSC Ensembl
chrY:13453753..13453753hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg385013
hg195013
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5618054
Supporting Variants
SamplesHG00096
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169727
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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