A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5871787



Internal ID9095629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73429583..73430858hg38UCSC Ensembl
chr6:74139306..74140581hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg381276
hg191276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2665458
Supporting Variants
SamplesHG01075
Known GenesMB21D1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5871787
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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