A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15191605



Internal ID21330474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33128044..33128044hg38UCSC Ensembl
chr10:33416972..33416972hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3948333
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15191605
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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