A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2750967



Internal ID12637833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:64321324..64492237hg38UCSC Ensembl
Innerchr10:66081084..66251994hg19UCSC Ensembl
Innerchr10:65751090..65922000hg18UCSC Ensembl
Innerchr10:65751090..65922000hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38170914
hg19170911
hg18170911
hg17170911
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6989752, essv6983197
SamplesBEC_554
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv2750967
Frequency
Sample Size771
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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