A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3770828



Internal ID18959028
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 StatusS
Merged Variantsnsv1071876
Supporting Variants
SamplesKWP1
Known GenesNFATC1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3770828
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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