A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013546



Internal ID19102764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:60594096..60702197hg38UCSC Ensembl
Innerchr4:61459814..61567915hg19UCSC Ensembl
Innerchr4:61142409..61250510hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38108102
hg19108102
hg18108102
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3739495
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)nsv1013546
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer