A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15756527



Internal ID22090998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42326676..42326676hg38UCSC Ensembl
chr4:42328693..42328693hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4441490
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15756527
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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