A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047446



Internal ID18789977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:105797401..106616713hg38UCSC Ensembl
Innerchr10:107557159..108376471hg19UCSC Ensembl
Innerchr10:107547149..108366461hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38819313
hg19819313
hg18819313
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3706219
Samples
Known GenesSORCS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047446
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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