A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002808



Internal ID19092025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:145723543..145777683hg38UCSC Ensembl
Innerchr3:145441330..145495470hg19UCSC Ensembl
Innerchr3:146924020..146978160hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3854141
hg1954141
hg1854141
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3741491
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)nsv1002808
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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