A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2789n106



Internal ID22796617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:48412311..48412551hg38UCSC Ensembl
chr4:48414328..48414568hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1134044, nsv1127273
SamplesKWS1
Known GenesSLAIN2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2789n106
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