A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17171115



Internal ID21431738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:8613272..8613272hg38UCSC Ensembl
chrY:8481313..8481313hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5605693
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17171115
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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