A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15190264



Internal ID21329113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:17653919..17653919hg38UCSC Ensembl
chr4:17655542..17655542hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3939613
Supporting Variants
SamplesHG002
Known GenesFAM184B
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15190264
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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