A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169636



Internal ID21462675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:15211540..15211540hg38UCSC Ensembl
chrY:17323420..17323420hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5605123
Supporting Variants
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169636
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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