A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4150n106



Internal ID22797978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130378213..130378713hg38UCSC Ensembl
chr9:133253600..133254100hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1113019, nsv1145268
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv4150n106
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