A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169472



Internal ID21447449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1408229..1410223hg38UCSC Ensembl
chrY:1477122..1479116hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg381995
hg191995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5667626
Supporting Variants
SamplesHG00732
Known GenesASMTL, ASMTL-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169472
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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