A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671841



Internal ID21620149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:326254..326813hg38UCSC Ensembl
chrY:236989..237548hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38560
hg19560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170683
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671841
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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