A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987979



Internal ID12972261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11416000..11575800hg38UCSC Ensembl
Innerchr9:11416000..11575800hg19UCSC Ensembl
Innerchr9:11406000..11565800hg18UCSC Ensembl
Innerchr9:11406000..11565800hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38159801
hg19159801
hg18159801
hg17159801
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752275
Supporting Variants
SamplesBEC_293
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987979
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