A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6990030



Internal ID12983599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:10785064..10886003hg38UCSC Ensembl
Innerchr7:10824691..10925630hg19UCSC Ensembl
Innerchr7:10791216..10892155hg18UCSC Ensembl
Innerchr7:10597931..10698870hg17UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38100940
hg19100940
hg18100940
hg17100940
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752139
Supporting Variants
SamplesSPC_183
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6990030
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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