A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv668n100



Internal ID22786755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6635558..6796980hg38UCSC Ensembl
chr10:6677520..6838942hg19UCSC Ensembl
chr10:6717526..6878948hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38161423
hg19161423
hg18161423
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046720, nsv1050602
Samples
Known GenesLINC00706, LINC00707
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv668n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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