A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169470



Internal ID21402111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1405243..1405309hg38UCSC Ensembl
chrY:1474136..1474202hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5669863
Supporting Variants
SamplesHG00096
Known GenesASMTL, ASMTL-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169470
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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