A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980206



Internal ID12981436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:153833267..154031267hg38UCSC Ensembl
Innerchr7:153530352..153728352hg19UCSC Ensembl
Innerchr7:153161285..153359285hg18UCSC Ensembl
Innerchr7:152968000..153166000hg17UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg38198001
hg19198001
hg18198001
hg17198001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34234
Supporting Variants
SamplesNA18968
Known GenesDPP6
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980206
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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