A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5599878



Internal ID21548515
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 StatusM
Merged Variants
Supporting Variantsnssv17162543
SamplesHG02492
Known GenesDMRT1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5599878
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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