A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013260



Internal ID19102478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:74147724..74255926hg38UCSC Ensembl
Innerchr4:75013441..75121643hg19UCSC Ensembl
Innerchr4:75232305..75340507hg18UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38108203
hg19108203
hg18108203
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5320n100
Supporting Variantsnssv3633822, nssv3633823, nssv3742869
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)nsv1013260
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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