A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658028



Internal ID9924133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:101034736..101039097hg38UCSC Ensembl
chr6:101482612..101486973hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg384362
hg194362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1146e199
Supporting Variantsessv5550791, essv6182662, essv5818297, essv5671203, essv6531852, essv6402563, essv5397997, essv6145798, essv5652625, essv6154061, essv6264220, essv5609440, essv6371839, essv5847031, essv6171106, essv6543796, essv6260890, essv5795998, essv6578988, essv5471586, essv6353318, essv5574072, essv6292873
SamplesNA18924, NA18861, NA19190, NA19107, NA19198, NA19138, NA18874, NA19207, NA19172, NA18520, NA18908, NA19152, NA19236, NA19114, NA18853, NA18523, NA18858, NA19108, NA19144, NA19248, NA18511, NA18522, NA18487
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658028
Frequency
Sample Size1151
Observed Gain0
Observed Loss23
Observed Complex0
Frequencyn/a


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