A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1072811



Internal ID19318022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74773268..74773353hg38UCSC Ensembl
chr18:72485224..72485309hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3762730
SamplesKWP1
Known GenesZNF407
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1072811
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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