A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3682n100



Internal ID22789769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56184913..56212669hg38UCSC Ensembl
chr19:56696282..56724038hg19UCSC Ensembl
chr19:61388094..61415850hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3827757
hg1927757
hg1827757
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1058259, nsv1059084
Samples
Known GenesGALP, ZSCAN5B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3682n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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