A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162452



Internal ID21481219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74086544..74086607hg38UCSC Ensembl
chr9:76701460..76701523hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591934
Supporting Variants
SamplesHG03683
Known GenesMIR6130
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162452
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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