A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15202242



Internal ID21341043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:115186378..115186378hg38UCSC Ensembl
chr5:114522075..114522075hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3934313
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15202242
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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