A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984841



Internal ID12983594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:10777460..10895936hg38UCSC Ensembl
Innerchr7:10817087..10935563hg19UCSC Ensembl
Innerchr7:10783612..10902088hg18UCSC Ensembl
Innerchr7:10590327..10708803hg17UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38118477
hg19118477
hg18118477
hg17118477
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 Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984841
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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