A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667303



Internal ID21615609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:56717656..56718595hg38UCSC Ensembl
chrY:58872276..58873215hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg38940
hg19940
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170845
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667303
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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