A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15201257



Internal ID21340057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:154850279..154850279hg38UCSC Ensembl
chr4:155771431..155771431hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3927979
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15201257
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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