A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987745



Internal ID12978099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:105858290..105913349hg38UCSC Ensembl
Innerchr10:107618048..107673107hg19UCSC Ensembl
Innerchr10:107608038..107663097hg18UCSC Ensembl
Innerchr10:107608038..107663097hg17UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3855060
hg1955060
hg1855060
hg1755060
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34654
Supporting Variants
SamplesNA06991
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987745
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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