A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050106



Internal ID18792637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:51515226..51540381hg38UCSC Ensembl
Innerchr10:53274986..53300141hg19UCSC Ensembl
Innerchr10:52944992..52970147hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3825156
hg1925156
hg1825156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3504878, nssv3518576, nssv3504883
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)nsv1050106
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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