A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036645



Internal ID18779176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:51045201..51399316hg38UCSC Ensembl
Innerchr10:52804961..53159076hg19UCSC Ensembl
Innerchr10:52474967..52829082hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38354116
hg19354116
hg18354116
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3505336
Samples
Known GenesMIR605, PRKG1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036645
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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