A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979295



Internal ID12979969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:82629847..82677437hg38UCSC Ensembl
Innerchr10:84389603..84437193hg19UCSC Ensembl
Innerchr10:84379583..84427173hg18UCSC Ensembl
Innerchr10:84379583..84427173hg17UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3847591
hg1947591
hg1847591
hg1747591
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35106
Supporting Variants
SamplesNA18524
Known GenesNRG3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979295
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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