A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979771



Internal ID12980717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:153833267..153960267hg38UCSC Ensembl
Innerchr7:153530352..153657352hg19UCSC Ensembl
Innerchr7:153161285..153288285hg18UCSC Ensembl
Innerchr7:152968000..153095000hg17UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg38127001
hg19127001
hg18127001
hg17127001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34787
Supporting Variants
SamplesNA18623
Known GenesDPP6
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979771
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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