A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162543



Internal ID21456457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:876913..876973hg38UCSC Ensembl
chr9:876913..876973hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5599878
Supporting Variants
SamplesHG02492
Known GenesDMRT1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162543
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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