A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15200031



Internal ID21338827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168835647..168835647hg38UCSC Ensembl
chr4:169756798..169756798hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3928706
Supporting Variants
SamplesHG002
Known GenesPALLD
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15200031
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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