A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17141687



Internal ID21402366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97939146..97939329hg38UCSC Ensembl
chr7:97568458..97568641hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5568922
Supporting Variants
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17141687
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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