A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15766750



Internal ID22101224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71387784..71387784hg38UCSC Ensembl
chr11:71098830..71098830hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4446389
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15766750
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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