A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665277



Internal ID9931382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:146770679..146773355hg38UCSC Ensembl
chr6:147091815..147094491hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg382677
hg192677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5847190, essv6126160, essv5779847, essv6446682, essv5792450
SamplesNA19087, NA19007, NA19084, NA19072, NA19085
Known GenesADGB
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665277
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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