A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170657



Internal ID21431608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:2891928..2891928hg38UCSC Ensembl
chrY:2759969..2759969hg19UCSC Ensembl
CytobandYp11.31
Allele length
AssemblyAllele length
hg38355
hg19355
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5605131
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170657
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer