A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1071281



Internal ID19326298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:27804578..27805779hg38UCSC Ensembl
chr16:27815899..27817100hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg381202
hg191202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3763955
SamplesKWP1
Known GenesGSG1L
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1071281
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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