A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1635n100



Internal ID22787722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:42629160..42651585hg38UCSC Ensembl
chr13:43203296..43225721hg19UCSC Ensembl
chr13:42101296..42123721hg18UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3822426
hg1922426
hg1822426
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1041476, nsv1043400
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1635n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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