A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659078



Internal ID9925183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:183660816..183661476hg38UCSC Ensembl
chr4:184581969..184582629hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38661
hg19661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6243319, essv5662185, essv6059093, essv6232844, essv5921793, essv5971781, essv6235082, essv6410379, essv6443151, essv6366092, essv6100874, essv6516564, essv5891928, essv5657708, essv5704400, essv6088708, essv6386514
SamplesHG01389, NA19660, NA20796, NA19681, HG01134, NA20278, NA19719, NA19087, HG00427, HG01136, HG01095, NA19682, NA19685, NA18628, HG01375, HG01491, NA18984
Known GenesTRAPPC11
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659078
Frequency
Sample Size1151
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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