A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162804



Internal ID21451161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74346380..74346380hg38UCSC Ensembl
chr9:76961296..76961296hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5639518
Supporting Variants
SamplesHG01505
Known GenesMIR6130
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162804
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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