A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15761638



Internal ID22096134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86110721..86110721hg38UCSC Ensembl
chr11:85821763..85821763hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38349
hg19349
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4446543
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15761638
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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