A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169274



Internal ID21474043
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 StatusS
Merged Variantsnsv5611319
Supporting Variants
SamplesHG03371
Known GenesASMT
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169274
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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