A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1625n100



Internal ID20153241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31678835..31773086hg38UCSC Ensembl
chr13:32252972..32347223hg19UCSC Ensembl
chr13:31150972..31245223hg18UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg3894252
hg1994252
hg1894252
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1042692, nsv1051962
Samples
Known GenesRXFP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1625n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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