A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007782



Internal ID19097001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:59520224..59684990hg38UCSC Ensembl
Innerchr4:60385942..60550708hg19UCSC Ensembl
Innerchr4:60068537..60233303hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38164767
hg19164767
hg18164767
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5220n100
Supporting Variantsnssv3626515
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)nsv1007782
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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