A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041537



Internal ID18784068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:51622469..51655047hg38UCSC Ensembl
Innerchr10:53382229..53414807hg19UCSC Ensembl
Innerchr10:53052235..53084813hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3832579
hg1932579
hg1832579
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3513160
Samples
Known GenesPRKG1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041537
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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