A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15765597



Internal ID22100081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:57350843..57350843hg38UCSC Ensembl
chr20:55925899..55925899hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4444214
Supporting Variants
Samples
Known GenesMIR5095
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15765597
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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