A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952923



Internal ID17301797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:12257944..12262643hg38UCSC Ensembl
Outerchr16:12351801..12356500hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg384700
hg194700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999221
SamplesBILGI_BIOE
Known GenesSNX29
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952923
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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