A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1072818



Internal ID19320385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:77184145..77185329hg38UCSC Ensembl
chr18:74896101..74897285hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381185
hg191185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764003
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1072818
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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