A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676893



Internal ID9942998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15841532..15847619hg38UCSC Ensembl
chr4:15843155..15849242hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg386088
hg196088
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6110283, essv5743479, essv6430359, essv5778026, essv6398222, essv5664069, essv5533968, essv5642717, essv5716086, essv5582919, essv6060581, essv6356662, essv5961923
SamplesNA19909, NA19704, NA19446, NA19313, NA18868, NA19445, NA19707, NA19982, NA18871, NA18499, NA18909, HG01375, NA19472
Known GenesCD38
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676893
Frequency
Sample Size1151
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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