A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979003



Internal ID12632782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:105128602..105512602hg38UCSC Ensembl
Innerchr7:104769049..105153049hg19UCSC Ensembl
Innerchr7:104556285..104940285hg18UCSC Ensembl
Innerchr7:104363000..104747000hg17UCSC Ensembl
Cytoband7q22.2
Allele length
AssemblyAllele length
hg38384001
hg19384001
hg18384001
hg17384001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34588
Supporting Variants
SamplesNA12814
Known GenesPUS7, SRPK2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979003
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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