A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674928



Internal ID9941033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24040879..24041300hg38UCSC Ensembl
chr1:24367369..24367790hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38422
hg19422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6028652, essv6120722, essv6086473, essv6150592, essv5966423, essv5776849, essv5607650, essv5873139, essv6551327, essv5932308, essv6447787, essv6414442, essv6371620, essv6250066, essv5708663
SamplesNA19703, NA19190, HG01365, HG01069, NA18868, NA19985, NA19114, NA19453, NA19318, NA19360, NA19398, NA18501, NA19093, NA19711, NA19430
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674928
Frequency
Sample Size1151
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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