A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988242



Internal ID12980716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:82814664..82858864hg38UCSC Ensembl
Innerchr10:84574420..84618620hg19UCSC Ensembl
Innerchr10:84564400..84608600hg18UCSC Ensembl
Innerchr10:84564400..84608600hg17UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3844201
hg1944201
hg1844201
hg1744201
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)essv6988242
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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