A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170766



Internal ID21508607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:56682260..56682824hg38UCSC Ensembl
chrY:58908047..58908611hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg38565
hg19565
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666468
Supporting Variants
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170766
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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