A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155273



Internal ID22085778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:21401082..21503752hg38UCSC Ensembl
Outerchr16:21378649..21503767hg38UCSC Ensembl
Innerchr16:21412403..21515073hg19UCSC Ensembl
Outerchr16:21389970..21515088hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38125119
hg19125119
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4011604, nssv4011605
Samples
Known GenesLOC100190986, LOC100271836, NPIPB3, SNX29P1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155273
Frequency
Sample Size131
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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