A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077813



Internal ID19320034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10697142..10725743hg38UCSC Ensembl
chr16:10790999..10819600hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3828602
hg1928602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764069
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077813
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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