A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5611319



Internal ID21559624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1633953..1633953hg38UCSC Ensembl
chrY:1702846..1702846hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg381020
hg191020
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169274
SamplesHG03371
Known GenesASMT
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5611319
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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