A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988872



Internal ID12637099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:68053842..68261586hg38UCSC Ensembl
Innerchr6:68763734..68971478hg19UCSC Ensembl
Innerchr6:68820455..69028199hg18UCSC Ensembl
Innerchr6:68820455..69028199hg17UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38207745
hg19207745
hg18207745
hg17207745
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752129
Supporting Variants
SamplesSPC_20
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988872
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