A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3506285



Internal ID18804566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:30564485..30581166hg38UCSC Ensembl
Innerchr10:30853414..30870095hg19UCSC Ensembl
Innerchr10:30893420..30910101hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3816682
hg1916682
hg1816682
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040895
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)nssv3506285
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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