A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170429



Internal ID21431507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:21670913..21670913hg38UCSC Ensembl
chrY:23832799..23832799hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5619069
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170429
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