A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038218



Internal ID19127437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:93968751..93991742hg38UCSC Ensembl
Innerchr10:95728508..95751499hg19UCSC Ensembl
Innerchr10:95718498..95741489hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3822992
hg1922992
hg1822992
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3508334
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)nsv1038218
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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