A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17171338



Internal ID21438942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:990641..990641hg38UCSC Ensembl
chrY:901376..901376hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38687
hg19687
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5614039
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17171338
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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