A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979706



Internal ID12980613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:7466152..7518982hg38UCSC Ensembl
Innerchr10:7508114..7560944hg19UCSC Ensembl
Innerchr10:7548120..7600950hg18UCSC Ensembl
Innerchr10:7548120..7600950hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3852831
hg1952831
hg1852831
hg1752831
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34803
Supporting Variants
SamplesNA18611
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979706
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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