A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170834



Internal ID21462540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:527097..527097hg38UCSC Ensembl
chrY:437832..437832hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg383281
hg193281
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5623057
Supporting Variants
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170834
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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