A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979700



Internal ID12980602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7272542..7368850hg38UCSC Ensembl
Innerchr9:7272542..7368850hg19UCSC Ensembl
Innerchr9:7262542..7358850hg18UCSC Ensembl
Innerchr9:7262542..7358850hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3896309
hg1996309
hg1896309
hg1796309
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)essv6979700
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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