A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012882



Internal ID19102099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:63255703..63428054hg38UCSC Ensembl
Innerchr4:64121421..64293772hg19UCSC Ensembl
Innerchr4:63804016..63976367hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38172352
hg19172352
hg18172352
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5225n100
Supporting Variantsnssv3626537, nssv3626539, nssv3626540, nssv3626538
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)nsv1012882
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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