A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668454



Internal ID21616759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:13118908..13120449hg38UCSC Ensembl
chrY:15230822..15232363hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg381542
hg191542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169258
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668454
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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