A curated catalogue of human genomic structural variation




Variant Details

Variant: esv34220



Internal ID12990259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7272542..7368850hg38UCSC Ensembl
Innerchr9:7272542..7368850hg19UCSC Ensembl
Innerchr9:7262542..7358850hg18UCSC Ensembl
Innerchr9:7262542..7358850hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3896309
hg1996309
hg1896309
hg1796309
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv256e55
Supporting Variantsessv6988221, essv6979701, essv6979700
SamplesNA18608
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv34220
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