A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3359n106



Internal ID22797187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107114496..107115696hg38UCSC Ensembl
chr6:107435700..107436900hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381201
hg191201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1112904, nsv1119086
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3359n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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