A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170767



Internal ID21508606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:56683455..56683664hg38UCSC Ensembl
chrY:58907207..58907416hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg38210
hg19210
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5668453
Supporting Variants
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170767
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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