A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979764



Internal ID12980713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:82778988..82858895hg38UCSC Ensembl
Innerchr10:84538744..84618651hg19UCSC Ensembl
Innerchr10:84528724..84608631hg18UCSC Ensembl
Innerchr10:84528724..84608631hg17UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3879908
hg1979908
hg1879908
hg1779908
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 Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979764
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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