A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029451



Internal ID19118670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:163920725..163950975hg38UCSC Ensembl
Innerchr4:164841877..164872127hg19UCSC Ensembl
Innerchr4:165061327..165091577hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3830251
hg1930251
hg1830251
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3634164
Samples
Known GenesMARCH1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029451
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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