A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984100



Internal ID12977670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:4438361..4605757hg38UCSC Ensembl
Innerchr7:4477992..4645388hg19UCSC Ensembl
Innerchr7:4444518..4611914hg18UCSC Ensembl
Innerchr7:4251233..4418629hg17UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38167397
hg19167397
hg18167397
hg17167397
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752157
Supporting Variants
SamplesBEC_774
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984100
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