A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4309n100



Internal ID20155925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38271961..38345891hg38UCSC Ensembl
chr20:36900363..36974294hg19UCSC Ensembl
chr20:36333777..36407708hg18UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3873931
hg1973932
hg1873932
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1065562, nsv1056405
Samples
Known GenesBPI, LOC149684
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4309n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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