A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766157



Internal ID18958927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37169423..37170324hg38UCSC Ensembl
chr6:37137199..37138100hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073549
Supporting Variants
SamplesKWP1
Known GenesPIM1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766157
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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