A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3566552



Internal ID18518147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:29964373..30020645hg38UCSC Ensembl
Innerchr19:30455280..30511552hg19UCSC Ensembl
Innerchr19:35147120..35203392hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3856273
hg1956273
hg1856273
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1067099
Supporting Variants
Samples
Known GenesURI1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3566552
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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