A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044477



Internal ID18787008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:68428357..68628622hg38UCSC Ensembl
Innerchr10:70188114..70388379hg19UCSC Ensembl
Innerchr10:69858120..70058385hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38200266
hg19200266
hg18200266
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3516163
Samples
Known GenesDNA2, SLC25A16, TET1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044477
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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