A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667839



Internal ID9933944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98347257..98347768hg38UCSC Ensembl
chr7:97976569..97977080hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38512
hg19512
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6058739, essv5578754, essv5722820, essv6522388
SamplesHG00634, HG00610, NA18608, HG00437
Known GenesBAIAP2L1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667839
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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