A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15761656



Internal ID22096159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:44876468..44876468hg38UCSC Ensembl
chr1:45342140..45342140hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38399
hg19399
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4445377
Supporting Variants
Samples
Known GenesEIF2B3
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15761656
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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