A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982195



Internal ID12626652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13222943..13597606hg38UCSC Ensembl
Innerchr21:14595264..14969927hg19UCSC Ensembl
Innerchr21:13517135..13891798hg18UCSC Ensembl
Innerchr21:13517135..13891798hg17UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38374664
hg19374664
hg18374664
hg17374664
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751923
Supporting Variants
SamplesBEC_401
Known GenesMIR3156-3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982195
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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