A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3566532



Internal ID18518127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:29961142..30018642hg38UCSC Ensembl
Innerchr19:30452049..30509549hg19UCSC Ensembl
Innerchr19:35143889..35201389hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3857501
hg1957501
hg1857501
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060537
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)nssv3566532
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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