A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988221



Internal ID12980604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7288704..7363648hg38UCSC Ensembl
Innerchr9:7288704..7363648hg19UCSC Ensembl
Innerchr9:7278704..7353648hg18UCSC Ensembl
Innerchr9:7278704..7353648hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3874945
hg1974945
hg1874945
hg1774945
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)essv6988221
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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