A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2735n100



Internal ID22788822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12627638..12643124hg38UCSC Ensembl
chr16:12721495..12736981hg19UCSC Ensembl
chr16:12628996..12644482hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3815487
hg1915487
hg1815487
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044212, nsv1048158
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)dgv2735n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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