A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1071255



Internal ID19318906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4116098..4116599hg38UCSC Ensembl
chr16:4166099..4166600hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3768097
SamplesKWP1
Known GenesADCY9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1071255
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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