A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2671n106



Internal ID20162028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194347571..194348271hg38UCSC Ensembl
chr3:194068300..194069000hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1126663, nsv1122074
SamplesKWS2, KWS1
Known GenesCPN2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2671n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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