A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037193



Internal ID19126412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:943593..973690hg38UCSC Ensembl
Innerchr10:989533..1019630hg19UCSC Ensembl
Innerchr10:979533..1009630hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3830098
hg1930098
hg1830098
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3484460
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)nsv1037193
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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