A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3646n100



Internal ID22789733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:53368137..53445339hg38UCSC Ensembl
chr19:53871390..53948592hg19UCSC Ensembl
chr19:58563202..58640404hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3877203
hg1977203
hg1877203
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1057295, nsv1060229
Samples
Known GenesTPM3P9, ZNF525, ZNF761, ZNF765
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3646n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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