A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16270882



Internal ID20480100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:55169803..55170195hg38UCSC Ensembl
chr7:55237496..55237888hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38393
hg19393
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749319
Supporting Variants
Samples
Known GenesEGFR
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16270882
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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