A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15761076



Internal ID22095572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:55166556..55166556hg38UCSC Ensembl
chr7:55234249..55234249hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38556
hg19556
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4444622
Supporting Variants
Samples
Known GenesEGFR
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15761076
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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