A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170993



Internal ID21508095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:56690486..56690776hg38UCSC Ensembl
chrY:58900095..58900385hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg38291
hg19291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5669041
Supporting Variants
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170993
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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