A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988210



Internal ID12633843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:19488140..19829015hg38UCSC Ensembl
Innerchr10:19777069..20117944hg19UCSC Ensembl
Innerchr10:19817075..20157950hg18UCSC Ensembl
Innerchr10:19817075..20157950hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38340876
hg19340876
hg18340876
hg17340876
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34306
Supporting Variants
SamplesNA18592
Known GenesPLXDC2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988210
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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