A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17145574



Internal ID21464330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100397002..100397708hg38UCSC Ensembl
chr9:103159284..103159990hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38707
hg19707
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5596266
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17145574
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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