A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170650



Internal ID21410369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:280877..280997hg38UCSC Ensembl
chrY:147544..147664hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5671642
Supporting Variants
SamplesHG00512
Known GenesPLCXD1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170650
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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