A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv462n106



Internal ID20159819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:59681395..59681486hg38UCSC Ensembl
chr10:61441153..61441244hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1111869, nsv1120638
SamplesKWS1, KWS2
Known GenesSLC16A9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv462n106
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