A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036247



Internal ID18778778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:12469909..12492299hg38UCSC Ensembl
Innerchr10:12511908..12534298hg19UCSC Ensembl
Innerchr10:12551914..12574304hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3822391
hg1922391
hg1822391
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv675n100
Supporting Variantsnssv3483488
Samples
Known GenesCAMK1D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036247
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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