A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3355n106



Internal ID20162712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:104774076..104774393hg38UCSC Ensembl
chr6:105221951..105222268hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1120885, nsv1130535
SamplesKWS2
Known GenesHACE1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3355n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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