A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170569



Internal ID21487548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:4980523..4980843hg38UCSC Ensembl
chrY:4848564..4848884hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5669914
Supporting Variants
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170569
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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