A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987035



Internal ID12981428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:153833323..154031059hg38UCSC Ensembl
Innerchr7:153530408..153728144hg19UCSC Ensembl
Innerchr7:153161341..153359077hg18UCSC Ensembl
Innerchr7:152968056..153165792hg17UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg38197737
hg19197737
hg18197737
hg17197737
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)essv6987035
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer