A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15757664



Internal ID22092141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73719828..73719828hg38UCSC Ensembl
chr14:74186531..74186531hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4445447
Supporting Variants
Samples
Known GenesELMSAN1
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=SIMPLEINS
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15757664
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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