A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170692



Internal ID21431580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:425443..425443hg38UCSC Ensembl
chrY:336178..336178hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5619801
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170692
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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