A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611705



Internal ID6998611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169044342..169048200hg38UCSC Ensembl
Innerchr6:169044342..169048200hg38UCSC Ensembl
Outerchr6:169044134..169048441hg38UCSC Ensembl
chr6:169444437..169448295hg19UCSC Ensembl
Innerchr6:169444437..169448295hg19UCSC Ensembl
Outerchr6:169444229..169448536hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg383859
hg193859
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12646410
SamplesNA19466
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611705
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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