A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1071863



Internal ID18973536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:75211544..75211845hg38UCSC Ensembl
chr18:72923499..72923800hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771793
SamplesKWP1
Known GenesTSHZ1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1071863
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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