A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006851



Internal ID19096069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:238978283..239058472hg38UCSC Ensembl
Innerchr1:239141583..239221772hg19UCSC Ensembl
Innerchr1:237208206..237288395hg18UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg3880190
hg1980190
hg1880190
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3705541
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)nsv1006851
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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