A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169606



Internal ID21455813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:12487834..12487834hg38UCSC Ensembl
chrY:14599634..14599634hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5604534
Supporting Variants
SamplesHG02492
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169606
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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