A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3569789



Internal ID18868070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:19827557..19851430hg38UCSC Ensembl
Innerchr19:19938366..19962239hg19UCSC Ensembl
Innerchr19:19799366..19823239hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg3823874
hg1923874
hg1823874
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065805
Supporting Variants
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)nssv3569789
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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