A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169471



Internal ID21470376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1408123..1408437hg38UCSC Ensembl
chrY:1477016..1477330hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5671785
Supporting Variants
SamplesHG03125
Known GenesASMTL, ASMTL-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169471
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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