A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989570



Internal ID12974447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:56048433..56081433hg38UCSC Ensembl
Innerchr10:57808194..57841194hg19UCSC Ensembl
Innerchr10:57478200..57511200hg18UCSC Ensembl
Innerchr10:57478200..57511200hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3833001
hg1933001
hg1833001
hg1733001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750966
Supporting Variants
SamplesBEC_520
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989570
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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