A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983056



Internal ID12628070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:31125097..31253973hg38UCSC Ensembl
Innerchr12:31278031..31406907hg19UCSC Ensembl
Innerchr12:31169298..31298174hg18UCSC Ensembl
Innerchr12:31169298..31298174hg17UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38128877
hg19128877
hg18128877
hg17128877
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751046
Supporting Variants
SamplesBEC_538
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983056
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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