A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1071876



Internal ID18972668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:79521499..79522800hg38UCSC Ensembl
chr18:77281499..77282800hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381302
hg191302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770828
SamplesKWP1
Known GenesNFATC1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1071876
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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