A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3516778



Internal ID18815059
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 StatusS
Merged Variantsnsv1047007
Supporting Variants
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)nssv3516778
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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