A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv227e55



Internal ID22761177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:65018008..65603718hg38UCSC Ensembl
chr7:64478386..65068631hg19UCSC Ensembl
chr7:64115821..64706066hg18UCSC Ensembl
chr7:63922536..64512781hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38585711
hg19590246
hg18590246
hg17590246
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv34341, esv2752167
SamplesSPC_13, NA11840
Known GenesCCT6P3, ZNF92
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)dgv227e55
Frequency
Sample Size771
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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