A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15768239



Internal ID22102714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76602139..76602139hg38UCSC Ensembl
chr11:76313183..76313183hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38202
hg19202
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4446395
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15768239
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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