A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17141466



Internal ID21401408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:76184258..76184945hg38UCSC Ensembl
chr7:75813576..75814263hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38688
hg19688
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5571231
Supporting Variants
SamplesHG00096
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17141466
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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