A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985678



Internal ID12627321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:52761343..52824743hg38UCSC Ensembl
Innerchr6:52626141..52689541hg19UCSC Ensembl
Innerchr6:52734100..52797500hg18UCSC Ensembl
Innerchr6:52734100..52797500hg17UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3863401
hg1963401
hg1863401
hg1763401
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752126
Supporting Variants
SamplesBEC_492
Known GenesGSTA1, GSTA2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985678
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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