A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15190646



Internal ID21329506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26109437..26109437hg38UCSC Ensembl
chr4:26111059..26111059hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3930725
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15190646
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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