A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070342



Internal ID19318854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:28211378..28211979hg38UCSC Ensembl
chr16:28222699..28223300hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770632
SamplesKWP1
Known GenesXPO6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070342
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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