A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3683n100



Internal ID20155299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56197884..56233260hg38UCSC Ensembl
chr19:56709253..56744629hg19UCSC Ensembl
chr19:61401065..61436441hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3835377
hg1935377
hg1835377
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1058119, nsv1065286
Samples
Known GenesZSCAN5A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3683n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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