A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3681n100



Internal ID20155297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55906849..56338089hg38UCSC Ensembl
chr19:56418215..56849458hg19UCSC Ensembl
chr19:61110027..61541270hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38431241
hg19431244
hg18431244
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1064371, nsv1057316
Samples
Known GenesGALP, NLRP13, NLRP5, NLRP8, ZNF444, ZNF787, ZSCAN5A, ZSCAN5B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3681n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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