A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1071261



Internal ID19319696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9495769..9495824hg38UCSC Ensembl
chr16:9589626..9589681hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3766772
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1071261
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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