A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15201243



Internal ID21340047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:151678620..151678620hg38UCSC Ensembl
chr4:152599772..152599772hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38362
hg19362
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3948677
Supporting Variants
SamplesHG002
Known GenesPET112
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15201243
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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