A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv574n106



Internal ID19018683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3217446..3222878hg38UCSC Ensembl
chr11:3238676..3244108hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg385433
hg195433
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1120649, nsv1135426
SamplesKWS2
Known GenesMRGPRG, MRGPRG-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv574n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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