A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155272



Internal ID22085777
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv110n97
Supporting Variantsnssv4011603, nssv4011602
Samples
Known GenesLOC100190986, LOC100271836, NPIPB3, SLC7A5P2, SNX29P1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155272
Frequency
Sample Size131
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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