A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054899



Internal ID19144118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:52370168..52511559hg38UCSC Ensembl
Innerchr15:52662365..52803756hg19UCSC Ensembl
Innerchr15:50449657..50591048hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38141392
hg19141392
hg18141392
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552404
Samples
Known GenesMYO5A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054899
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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