A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660336



Internal ID9926441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85208788..85208921hg38UCSC Ensembl
chr16:85242394..85242527hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5741016, essv6046508, essv6427465, essv6509405, essv6556036, essv5703531, essv5841163, essv6387720, essv6067190, essv5537889, essv5847710, essv6038295, essv6478698, essv6191544, essv5782362, essv5786109, essv5504393, essv6451438, essv5546641, essv6042722, essv6445214
SamplesHG00318, NA18530, HG00261, HG00138, HG01070, HG00346, HG00281, HG00309, NA18613, HG00320, HG00533, HG00275, HG00324, HG00250, HG00276, HG00704, HG00246, HG00285, HG00256, HG00310, NA18612
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660336
Frequency
Sample Size1151
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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