A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv481n106



Internal ID20159838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:77041144..77041527hg38UCSC Ensembl
chr10:78800902..78801285hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38384
hg19384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1129891, nsv1111870
SamplesKWS1, KWS2
Known GenesKCNMA1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv481n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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