A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169946



Internal ID21488378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1681741..1681741hg38UCSC Ensembl
chrY:1750634..1750634hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5618770
Supporting Variants
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169946
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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