A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170790



Internal ID21431645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:626379..626584hg38UCSC Ensembl
chrY:537114..537319hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666733
Supporting Variants
SamplesHG00731
Known GenesSHOX
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170790
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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