A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980356



Internal ID12978249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:19375920..19494213hg38UCSC Ensembl
Innerchr7:19415543..19533836hg19UCSC Ensembl
Innerchr7:19382068..19500361hg18UCSC Ensembl
Innerchr7:19188783..19307076hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38118294
hg19118294
hg18118294
hg17118294
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34500
Supporting Variants
SamplesNA07345
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980356
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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