A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979766



Internal ID12980711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:82837764..82857164hg38UCSC Ensembl
Innerchr10:84597520..84616920hg19UCSC Ensembl
Innerchr10:84587500..84606900hg18UCSC Ensembl
Innerchr10:84587500..84606900hg17UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3819401
hg1919401
hg1819401
hg1719401
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34368
Supporting Variants
SamplesNA18623
Known GenesNRG3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979766
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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