A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15199957



Internal ID21338757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:64975413..64975413hg38UCSC Ensembl
chr4:65841131..65841131hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3926089
Supporting Variants
SamplesHG002
Known GenesLOC401134
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15199957
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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