A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007865



Internal ID19097084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12269..43111hg38UCSC Ensembl
Innerchr4:12269..43112hg19UCSC Ensembl
Innerchr4:2269..33112hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3830843
hg1930844
hg1830844
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5053n100
Supporting Variantsnssv3617109, nssv3617120, nssv3617114, nssv3617113, nssv3617111, nssv3617107, nssv3617110, nssv3617116, nssv3617112, nssv3617117, nssv3617106, nssv3617104, nssv3617115, nssv3617119, nssv3617105, nssv3617108, nssv3617118
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)nsv1007865
Frequency
Sample Size11257
Observed Gain14
Observed Loss3
Observed Complex0
Frequencyn/a


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