A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066978



Internal ID19156197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:24196288..24321291hg38UCSC Ensembl
Innerchr19:24379090..24504093hg19UCSC Ensembl
Innerchr19:24170930..24295933hg18UCSC Ensembl
Cytoband19p11
Allele length
AssemblyAllele length
hg38125004
hg19125004
hg18125004
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3485n100
Supporting Variantsnssv3570680
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)nsv1066978
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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