A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2752310



Internal ID12985862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7260390..7390841hg38UCSC Ensembl
Innerchr9:7260390..7390841hg19UCSC Ensembl
Innerchr9:7250390..7380841hg18UCSC Ensembl
Innerchr9:7250390..7380841hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38130452
hg19130452
hg18130452
hg17130452
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv256e55
Supporting Variantsessv6983548, essv6989811, essv6983547, essv6989812
SamplesBEC_667
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)esv2752310
Frequency
Sample Size771
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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