A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668218



Internal ID9587637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6758435..6758720hg38UCSC Ensembl
chr17:6661754..6662039hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38286
hg19286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5828582, essv6342263, essv6057607, essv5548584
SamplesNA20332, NA19374, NA18520, NA19360
Known GenesXAF1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668218
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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