A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058675



Internal ID19147894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:28299338..28324239hg38UCSC Ensembl
Innerchr19:28790245..28815146hg19UCSC Ensembl
Innerchr19:33482085..33506986hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3824902
hg1924902
hg1824902
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3566524
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)nsv1058675
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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