A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1000063



Internal ID19089280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:107130169..107155364hg38UCSC Ensembl
Innerchr4:108051326..108076521hg19UCSC Ensembl
Innerchr4:108270775..108295970hg18UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3825196
hg1925196
hg1825196
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3632414
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)nsv1000063
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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