A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv387n106



Internal ID19018496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29423216..29423791hg38UCSC Ensembl
chr10:29712145..29712720hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38576
hg19576
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1133367, nsv1109270
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv387n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer