A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv256e55



Internal ID22761206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:7260390..7390841hg38UCSC Ensembl
chr9:7260390..7390841hg19UCSC Ensembl
chr9:7250390..7380841hg18UCSC Ensembl
chr9:7250390..7380841hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38130452
hg19130452
hg18130452
hg17130452
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2752310, esv34220
SamplesBEC_667, NA18608
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)dgv256e55
Frequency
Sample Size771
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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