A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4011601



Internal ID22073232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:21378649..21580019hg38UCSC Ensembl
Outerchr16:21368130..21582134hg38UCSC Ensembl
Innerchr16:21389970..21591340hg19UCSC Ensembl
Outerchr16:21379451..21593455hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38214005
hg19214005
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155271
Supporting Variants
Samples
Known GenesLOC100190986, LOC100271836, NPIPB3, SLC7A5P2, SNX29P1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4011601
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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