A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987488



Internal ID12977678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:4446308..4605758hg38UCSC Ensembl
Innerchr7:4485939..4645389hg19UCSC Ensembl
Innerchr7:4452465..4611915hg18UCSC Ensembl
Innerchr7:4259180..4418630hg17UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38159451
hg19159451
hg18159451
hg17159451
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)essv6987488
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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