A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030944



Internal ID19120164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:66709180..66735476hg38UCSC Ensembl
Innerchr5:66005008..66031304hg19UCSC Ensembl
Innerchr5:66040764..66067060hg18UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3826297
hg1926297
hg1826297
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3747234
Samples
Known GenesMAST4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030944
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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