A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979573



Internal ID12980394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:62751852..62798635hg38UCSC Ensembl
Innerchr5:62047679..62094462hg19UCSC Ensembl
Innerchr5:62083435..62130218hg18UCSC Ensembl
Innerchr5:62083435..62130218hg17UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3846784
hg1946784
hg1846784
hg1746784
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34525
Supporting Variants
SamplesNA18572
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979573
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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