A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056482



Internal ID19145701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:34120844..34164142hg38UCSC Ensembl
Innerchr19:34611749..34655047hg19UCSC Ensembl
Innerchr19:39303589..39346887hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3843299
hg1943299
hg1843299
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3566585
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)nsv1056482
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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