A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4011602



Internal ID22073233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:21378649..21582313hg38UCSC Ensembl
Outerchr16:21368130..21584992hg38UCSC Ensembl
Innerchr16:21389970..21593634hg19UCSC Ensembl
Outerchr16:21379451..21596313hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38216863
hg19216863
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155272
Supporting Variants
Samples
Known GenesLOC100190986, LOC100271836, NPIPB3, SLC7A5P2, SNX29P1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4011602
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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