A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170884



Internal ID21472982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:56830932..56836965hg38UCSC Ensembl
chrY:58977079..58983112hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg386034
hg196034
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5671569
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170884
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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