A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170415



Internal ID21487300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:21549394..21549443hg38UCSC Ensembl
chrY:23711280..23711329hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5672096
Supporting Variants
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170415
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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