A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987832



Internal ID12625119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:38545256..38578378hg38UCSC Ensembl
Innerchr21:39917180..39950302hg19UCSC Ensembl
Innerchr21:38839050..38872172hg18UCSC Ensembl
Innerchr21:38839050..38872172hg17UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3833123
hg1933123
hg1833123
hg1733123
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751930
Supporting Variants
SamplesBEC_104
Known GenesERG
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987832
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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