A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671745



Internal ID9591164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3406304..3406438hg38UCSC Ensembl
chr19:3406302..3406436hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5715448, essv6177811, essv6182268, essv5646708, essv6587740, essv5700658, essv5589598, essv6301489, essv5903846, essv5965738, essv6337366, essv6179571, essv5854797, essv6085071, essv6082765, essv6430670, essv6242165, essv5765449, essv5603565, essv6226827, essv6123854, essv5987760, essv6147536, essv5588307
SamplesHG00257, HG01353, HG01052, NA19114, HG01173, HG01389, HG00326, HG00111, HG00256, HG00342, HG00140, HG01048, HG01183, HG00315, HG01187, HG01073, HG00273, HG00249, HG00329, NA19371, HG01108, HG01374, HG00345, HG00271
Known GenesNFIC
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671745
Frequency
Sample Size1151
Observed Gain0
Observed Loss24
Observed Complex0
Frequencyn/a


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