A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15762197



Internal ID22096693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1533765..1533765hg38UCSC Ensembl
chr6:1534000..1534000hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4438988
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15762197
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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