A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050663



Internal ID19139882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5696016..5743955hg38UCSC Ensembl
Innerchr10:5737979..5785918hg19UCSC Ensembl
Innerchr10:5777985..5825924hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3847940
hg1947940
hg1847940
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3497201
Samples
Known GenesFAM208B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050663
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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