A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15767597



Internal ID22102068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:180859067..180859067hg38UCSC Ensembl
chr1:180828203..180828203hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4448480
Supporting Variants
Samples
Known GenesXPR1
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15767597
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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