A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672928



Internal ID9592347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:95177152..95184582hg38UCSC Ensembl
chr13:95829406..95836836hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg387431
hg197431
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5837344, essv6225649, essv5611566, essv6440142
SamplesNA18541, NA12058, NA19062, HG01125
Known GenesABCC4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672928
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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