A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980679



Internal ID12625116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:38558606..38578406hg38UCSC Ensembl
Innerchr21:39930530..39950330hg19UCSC Ensembl
Innerchr21:38852400..38872200hg18UCSC Ensembl
Innerchr21:38852400..38872200hg17UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3819801
hg1919801
hg1819801
hg1719801
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)essv6980679
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer