A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2752166



Internal ID12985718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:65018008..65778609hg38UCSC Ensembl
Innerchr7:64478386..65243596hg19UCSC Ensembl
Innerchr7:64115821..64881031hg18UCSC Ensembl
Innerchr7:63922536..64687746hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38760602
hg19765211
hg18765211
hg17765211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv226e55
Supporting Variantsessv6984234, essv6984233, essv6989934
SamplesBEC_814
Known GenesCCT6P1, CCT6P3, INTS4L2, LOC441242, SNORA22, ZNF92
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv2752166
Frequency
Sample Size771
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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