A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004706



Internal ID19093923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:74149053..74255926hg38UCSC Ensembl
Innerchr4:75014770..75121643hg19UCSC Ensembl
Innerchr4:75233634..75340507hg18UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38106874
hg19106874
hg18106874
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5320n100
Supporting Variantsnssv3633825
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)nsv1004706
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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