A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989811



Internal ID12976455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7260390..7373868hg38UCSC Ensembl
Innerchr9:7260390..7373868hg19UCSC Ensembl
Innerchr9:7250390..7363868hg18UCSC Ensembl
Innerchr9:7250390..7363868hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38113479
hg19113479
hg18113479
hg17113479
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752310
Supporting Variants
SamplesBEC_667
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989811
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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