A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3413n106



Internal ID20162770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:152068854..152071265hg38UCSC Ensembl
chr6:152389989..152392400hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg382412
hg192412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1121042, nsv1112142
SamplesKWS2
Known GenesESR1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3413n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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