A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3572028



Internal ID18870309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..27596469hg38UCSC Ensembl
Innerchr19:27747981..28087377hg19UCSC Ensembl
Innerchr19:32439821..32779217hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38339397
hg19339397
hg18339397
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062077
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)nssv3572028
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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