A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952922



Internal ID16955109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:11653545..11678444hg38UCSC Ensembl
Outerchr16:11747401..11772300hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3824900
hg1924900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999220
SamplesBILGI_BIOE
Known GenesSNN
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952922
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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