A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169788



Internal ID21480221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1314611..1314705hg38UCSC Ensembl
chrY:1383504..1383598hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5670865
Supporting Variants
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169788
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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