A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15205806



Internal ID21344604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:12513433..12513433hg38UCSC Ensembl
chrY:14625233..14625233hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3931791
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15205806
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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