A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026744



Internal ID18769275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:163555088..163994342hg38UCSC Ensembl
Innerchr4:164476240..164915494hg19UCSC Ensembl
Innerchr4:164695690..165134944hg18UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg38439255
hg19439255
hg18439255
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3634157
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)nsv1026744
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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