A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170855



Internal ID21508005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:56728663..56729000hg38UCSC Ensembl
chrY:58861871..58862208hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5672041
Supporting Variants
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170855
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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