A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608377



Internal ID6648616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25129951..25137230hg38UCSC Ensembl
Innerchr6:25130001..25137180hg38UCSC Ensembl
Outerchr6:25129901..25137280hg38UCSC Ensembl
chr6:25130179..25137458hg19UCSC Ensembl
Innerchr6:25130229..25137408hg19UCSC Ensembl
Outerchr6:25130129..25137508hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg387280
hg197280
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12232201
SamplesHG01685
Known GenesCMAHP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608377
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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