A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169637



Internal ID21473450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:15212506..15212506hg38UCSC Ensembl
chrY:17324386..17324386hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg38495
hg19495
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5617887
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169637
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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