A curated catalogue of human genomic structural variation




Variant Details

Variant: esv34777



Internal ID12990813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121672332..121701496hg38UCSC Ensembl
Innerchr10:123431846..123461010hg19UCSC Ensembl
Innerchr10:123421836..123451000hg18UCSC Ensembl
Innerchr10:123421836..123451000hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3829165
hg1929165
hg1829165
hg1729165
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6978718, essv6988036, essv6989040
SamplesNA12156
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv34777
Frequency
Sample Size771
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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