A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15765928



Internal ID22100399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156004603..156004603hg38UCSC Ensembl
chr1:155974394..155974394hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4445007
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15765928
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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