A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015999



Internal ID19105217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:170321770..170368212hg38UCSC Ensembl
Innerchr4:171242921..171289363hg19UCSC Ensembl
Innerchr4:171479496..171525938hg18UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg3846443
hg1946443
hg1846443
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5469n100
Supporting Variantsnssv3635385, nssv3635386, nssv3635387
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)nsv1015999
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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