A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980742



Internal ID12971920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:55875052..56019469hg38UCSC Ensembl
Innerchr10:57634812..57779230hg19UCSC Ensembl
Innerchr10:57304818..57449236hg18UCSC Ensembl
Innerchr10:57304818..57449236hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38144418
hg19144419
hg18144419
hg17144419
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750965
Supporting Variants
SamplesBEC_131
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980742
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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