A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1071864



Internal ID19326158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76494243..76495344hg38UCSC Ensembl
chr18:74206199..74207300hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381102
hg191102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3768818
SamplesKWP1
Known GenesZNF516
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1071864
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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