A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162829



Internal ID21428814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75383647..75383736hg38UCSC Ensembl
chr9:77998563..77998652hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5603577
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162829
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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