A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989254



Internal ID12972478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:22509514..22558702hg38UCSC Ensembl
Innerchr3:22551005..22600193hg19UCSC Ensembl
Innerchr3:22526009..22575197hg18UCSC Ensembl
Innerchr3:22526009..22575197hg17UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3849189
hg1949189
hg1849189
hg1749189
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751995
Supporting Variants
SamplesBEC_312
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989254
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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