A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17517027



Internal ID22574990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:10130568..10134518hg38UCSC Ensembl
chrY:9968177..9972127hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg383951
hg193951
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5977853
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17517027
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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