A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2804n106



Internal ID22796632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:58562830..58569373hg38UCSC Ensembl
chr4:59428995..59435538hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg386544
hg196544
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1127281, nsv1111641, nsv1112067
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2804n106
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