A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738429



Internal ID162095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:13458747..13464032hg38UCSC Ensembl
chrY:15570627..15575912hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg385286
hg195286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5433897
Supporting Variants
Samples
Known GenesUTY
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738429
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000626174


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