A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv261e55



Internal ID20126740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:38459766..38683303hg38UCSC Ensembl
chr9:38459763..38683300hg19UCSC Ensembl
chr9:38449763..38673300hg18UCSC Ensembl
chr9:38449763..38673300hg17UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38223538
hg19223538
hg18223538
hg17223538
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv34705, esv35073
SamplesNA12872, NA12864
Known GenesANKRD18A, FAM201A, FAM95C
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)dgv261e55
Frequency
Sample Size771
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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