A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982066



Internal ID12974358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17965725..18036894hg38UCSC Ensembl
Innerchr9:17965723..18036892hg19UCSC Ensembl
Innerchr9:17955723..18026892hg18UCSC Ensembl
Innerchr9:17955723..18026892hg17UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3871170
hg1971170
hg1871170
hg1771170
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752288
Supporting Variants
SamplesBEC_516
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982066
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