A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170873



Internal ID21451460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:56764274..56764558hg38UCSC Ensembl
chrY:58826313..58826597hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg38285
hg19285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5672427
Supporting Variants
SamplesHG01505
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170873
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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