A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv639e199



Internal ID22758412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37849605..37856002hg38UCSC Ensembl
chr19:38340245..38346642hg19UCSC Ensembl
Cytoband19q13.13
Allele length
AssemblyAllele length
hg386398
hg196398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2662482, esv2667801
SamplesHG00096, HG00249, HG00361, HG00315, HG00151, HG00150, HG00261, HG00327, HG00127, HG00251, HG00122, HG00185, HG00158, HG00281, HG00106, HG00325, HG00262, HG00309, HG00160, HG00326, HG00260, HG00176, HG00328, HG00368, HG00320, HG00246, HG00254, HG00336, HG00256, HG00269, HG00342, HG00343, HG00372, HG00180
Known GenesLOC100631378
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv639e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss34
Observed Complex0
Frequencyn/a


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