A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5377n100



Internal ID20156993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121352476..121370988hg38UCSC Ensembl
chr4:122273631..122292143hg19UCSC Ensembl
chr4:122493081..122511593hg18UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3818513
hg1918513
hg1818513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1014710, nsv1003747
Samples
Known GenesQRFPR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5377n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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