A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2752273



Internal ID12985825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:1062218..1824888hg38UCSC Ensembl
Innerchr9:1062218..1824888hg19UCSC Ensembl
Innerchr9:1052218..1814888hg18UCSC Ensembl
Innerchr9:1052218..1814888hg17UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38762671
hg19762671
hg18762671
hg17762671
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6986287, essv6982857, essv6988594, essv6986286
SamplesBEC_605
Known Genes
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)esv2752273
Frequency
Sample Size771
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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