A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671999



Internal ID21620304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:280560..280880hg38UCSC Ensembl
chrY:147227..147547hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170647
SamplesHG02818
Known GenesPLCXD1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671999
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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