A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952916



Internal ID17301790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:8850744..8864643hg38UCSC Ensembl
Outerchr16:8944601..8958500hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3813900
hg1913900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999213
SamplesBILGI_BIOE
Known GenesCARHSP1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952916
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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