A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3771822



Internal ID18960599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:23135335..23136236hg38UCSC Ensembl
chr18:20715299..20716200hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071838
Supporting Variants
SamplesKWP1
Known GenesCABLES1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3771822
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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