A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070361



Internal ID18972343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:83967394..83968795hg38UCSC Ensembl
chr16:84000999..84002400hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg381402
hg191402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3763143
SamplesKWP1
Known GenesNECAB2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070361
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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