A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3768724



Internal ID19308193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59590949..59591287hg38UCSC Ensembl
chr18:57258181..57258519hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071853
Supporting Variants
SamplesKWP1
Known GenesCCBE1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3768724
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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