A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665588



Internal ID21613893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:11174203..11174257hg38UCSC Ensembl
chrY:13329879..13329933hg19UCSC Ensembl
CytobandYq11.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169396
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665588
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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