A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169206



Internal ID21404608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1251401..1251484hg38UCSC Ensembl
chrY:1320294..1320377hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666635
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169206
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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