A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772248



Internal ID18962323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:55587568..55588369hg38UCSC Ensembl
chr18:53254799..53255600hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072268
Supporting Variants
SamplesKWP1
Known GenesTCF4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772248
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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