A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3577n100



Internal ID22789664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:42920507..43266414hg38UCSC Ensembl
chr19:43424659..43770566hg19UCSC Ensembl
chr19:48116499..48462406hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38345908
hg19345908
hg18345908
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1061205, nsv1058506, nsv1063695, nsv1056033, nsv1062617, nsv1063260, nsv1055880, nsv1061430
Samples
Known GenesLOC284344, PSG11, PSG2, PSG4, PSG5, PSG7, PSG9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3577n100
Frequency
Sample Size11257
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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