A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001852



Internal ID19091069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:77214721..77339116hg38UCSC Ensembl
Innerchr4:78135874..78260269hg19UCSC Ensembl
Innerchr4:78354898..78479293hg18UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38124396
hg19124396
hg18124396
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5322n100
Supporting Variantsnssv3633838
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)nsv1001852
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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