A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983651



Internal ID12976639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:111702290..111732214hg38UCSC Ensembl
Innerchr6:112023493..112053417hg19UCSC Ensembl
Innerchr6:112130186..112160110hg18UCSC Ensembl
Innerchr6:112130186..112160110hg17UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3829925
hg1929925
hg1829925
hg1729925
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752088
Supporting Variants
SamplesBEC_676
Known GenesFYN
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983651
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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