A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664718



Internal ID21613024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:23658543..23658959hg38UCSC Ensembl
chrY:25804690..25805106hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38417
hg19417
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17171158
SamplesHG01505
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664718
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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