A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17148283



Internal ID21459913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:4768111..4768430hg38UCSC Ensembl
chr7:4807742..4808061hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5570799
Supporting Variants
SamplesHG02818
Known GenesFOXK1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17148283
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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