A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672032



Internal ID9938137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89325093..89325195hg38UCSC Ensembl
chr15:89868324..89868426hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6165655, essv5850718, essv6070436, essv6011932, essv6473913, essv6591408, essv5687455, essv5919027, essv5985760, essv6023712, essv5827048, essv6557023, essv5730025, essv6452158, essv5473809, essv5959243, essv5699988, essv5488716, essv6267168, essv5774967, essv5573746, essv6436934, essv5836834, essv5537570, essv6352754, essv5600761, essv5593733, essv5718388, essv5502026, essv6389943, essv6088877, essv5539843, essv6488175, essv5508639, essv5798355, essv5401173
SamplesNA11830, HG01521, HG00524, NA18980, HG01188, HG01066, NA18959, NA18606, HG00327, NA18595, HG00512, HG00335, HG01440, HG01048, HG00419, NA11993, HG00313, HG00443, NA19070, HG00732, HG00436, HG00275, HG00284, HG01073, HG00273, NA18856, NA18555, NA18536, NA18632, HG00336, NA18543, NA12763, NA12749, NA18609, NA20502, HG01061
Known GenesPOLG
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672032
Frequency
Sample Size1151
Observed Gain0
Observed Loss36
Observed Complex0
Frequencyn/a


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