A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3600n100



Internal ID22789687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43208086..43252073hg38UCSC Ensembl
chr19:43712238..43756225hg19UCSC Ensembl
chr19:48404078..48448065hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3843988
hg1943988
hg1843988
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1060308, nsv1056342, nsv1060009
Samples
Known GenesLOC284344
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3600n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss87
Observed Complex0
Frequencyn/a


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