A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3724337



Internal ID18675932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27257073..27782693hg38UCSC Ensembl
Innerchr19:27747981..28273601hg19UCSC Ensembl
Innerchr19:32439821..32965441hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38525621
hg19525621
hg18525621
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066699
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)nssv3724337
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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