A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17171017



Internal ID21402032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:6441411..6441411hg38UCSC Ensembl
chrY:6309452..6309452hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg384000
hg194000
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5619994
Supporting Variants
SamplesHG00096
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17171017
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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