A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15760795



Internal ID22095286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10902540..10902540hg38UCSC Ensembl
chr2:11042666..11042666hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4446066
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15760795
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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