A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15200707



Internal ID21339503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39408925..39408925hg38UCSC Ensembl
chr4:39410545..39410545hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3947643
Supporting Variants
SamplesHG002
Known GenesKLB, MIR1273H
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15200707
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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