A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169258



Internal ID21511774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:13118908..13120449hg38UCSC Ensembl
chrY:15230822..15232363hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg381542
hg191542
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5668454
Supporting Variants
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169258
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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