A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15200979



Internal ID21339788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17883915..17883915hg38UCSC Ensembl
chr5:17884024..17884024hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3940112
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15200979
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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