A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5612947



Internal ID21561252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:21295196..21295196hg38UCSC Ensembl
chrY:23457082..23457082hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38813
hg19813
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170404
SamplesHG01505
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5612947
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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