A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064389



Internal ID19153608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:56233260..56256863hg38UCSC Ensembl
Innerchr19:56744629..56768232hg19UCSC Ensembl
Innerchr19:61436441..61460044hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3823604
hg1923604
hg1823604
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3570448
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)nsv1064389
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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