A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987996



Internal ID12972471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:22520505..22558705hg38UCSC Ensembl
Innerchr3:22561996..22600196hg19UCSC Ensembl
Innerchr3:22537000..22575200hg18UCSC Ensembl
Innerchr3:22537000..22575200hg17UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3838201
hg1938201
hg1838201
hg1738201
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)essv6987996
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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