A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987034



Internal ID12981429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:153827793..153948014hg38UCSC Ensembl
Innerchr7:153524878..153645099hg19UCSC Ensembl
Innerchr7:153155811..153276032hg18UCSC Ensembl
Innerchr7:152962526..153082747hg17UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg38120222
hg19120222
hg18120222
hg17120222
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 Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987034
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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