A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979701



Internal ID12980603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7288700..7363650hg38UCSC Ensembl
Innerchr9:7288700..7363650hg19UCSC Ensembl
Innerchr9:7278700..7353650hg18UCSC Ensembl
Innerchr9:7278700..7353650hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3874951
hg1974951
hg1874951
hg1774951
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34220
Supporting Variants
SamplesNA18608
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979701
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