A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17146405



Internal ID21498521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:106445404..106445475hg38UCSC Ensembl
chr7:106085850..106085921hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5580113
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17146405
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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