A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010999



Internal ID18753532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:988303..998325hg38UCSC Ensembl
Innerchr3:1029987..1040009hg19UCSC Ensembl
Innerchr3:1004987..1015009hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3810023
hg1910023
hg1810023
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3590292
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)nsv1010999
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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