A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3249n106



Internal ID20162606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:675498..675680hg38UCSC Ensembl
chr6:675498..675680hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1134646, nsv1116373
SamplesKWS1
Known GenesEXOC2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3249n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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