A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074388



Internal ID18977940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28510222..29115423hg38UCSC Ensembl
chr6:28477999..29083200hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38605202
hg19605202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772199
SamplesKWP1
Known GenesC6orf100, GPX5, GPX6, HCG14, LOC100129636, LOC401242, OR2B3, OR2J3, OR2W1, SCAND3, TRIM27, ZNF311
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074388
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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