A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17146716



Internal ID21498393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:45083587..45083826hg38UCSC Ensembl
chr7:45123186..45123425hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38240
hg19240
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5565194
Supporting Variants
SamplesNA19239
Known GenesNACAD
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17146716
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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