A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5320n100



Internal ID22791407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:74147724..74265726hg38UCSC Ensembl
chr4:75013441..75131443hg19UCSC Ensembl
chr4:75232305..75350307hg18UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38118003
hg19118003
hg18118003
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1004706, nsv1013260, nsv1002907
Samples
Known GenesMTHFD2L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5320n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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