A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063592



Internal ID18806123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:38767337..38796625hg38UCSC Ensembl
Innerchr19:39257977..39287265hg19UCSC Ensembl
Innerchr19:43949817..43979105hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3829289
hg1929289
hg1829289
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3568203
Samples
Known GenesLGALS7, LGALS7B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063592
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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