A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3706191



Internal ID18657786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:90324175..90700158hg38UCSC Ensembl
Innerchr10:92083932..92459915hg19UCSC Ensembl
Innerchr10:92073912..92449895hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38375984
hg19375984
hg18375984
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036256
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)nssv3706191
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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