A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170819



Internal ID21473156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:3795155..3795155hg38UCSC Ensembl
chrY:3663196..3663196hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38383
hg19383
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5615412
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170819
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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