A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041360



Internal ID19130579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121129041..121206408hg38UCSC Ensembl
Innerchr10:122888555..122965922hg19UCSC Ensembl
Innerchr10:122878545..122955912hg18UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3877368
hg1977368
hg1877368
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3706244
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)nsv1041360
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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