A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034844



Internal ID19124065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:16854232..16902991hg38UCSC Ensembl
Innerchr5:16854341..16903100hg19UCSC Ensembl
Innerchr5:16907341..16956100hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3848760
hg1948760
hg1848760
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3638304
Samples
Known GenesMYO10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034844
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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