A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047007



Internal ID19136226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:91106094..91150962hg38UCSC Ensembl
Innerchr10:92865851..92910719hg19UCSC Ensembl
Innerchr10:92855831..92900699hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3844869
hg1944869
hg1844869
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv953n100
Supporting Variantsnssv3516778
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047007
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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