A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170844



Internal ID21508250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:56715341..56715610hg38UCSC Ensembl
chrY:58875261..58875530hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665568
Supporting Variants
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170844
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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