A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979292



Internal ID12979947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20457265..20610665hg38UCSC Ensembl
Innerchr10:20746194..20899594hg19UCSC Ensembl
Innerchr10:20786200..20939600hg18UCSC Ensembl
Innerchr10:20786200..20939600hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38153401
hg19153401
hg18153401
hg17153401
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34621
Supporting Variants
SamplesNA18524
Known GenesMIR4675
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979292
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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