A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664992



Internal ID21613297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:7149956..7150057hg38UCSC Ensembl
chrY:7017997..7018098hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17171061
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664992
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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