A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15768136



Internal ID22102611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54594299..54594299hg38UCSC Ensembl
chr8:55506859..55506859hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4449217
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15768136
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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