A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17029178



Internal ID87149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11732000..11737825hg38UCSC Ensembl
chr10:11773999..11779824hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg385826
hg195826
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142101
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17029178
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000461


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