A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608077



Internal ID6648316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10522451..10553306hg38UCSC Ensembl
chr6:10522684..10553539hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg3830856
hg1930856
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1165e214
Supporting Variantsessv12188406, essv12188405
SamplesHG03857, HG02292
Known GenesGCNT2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608077
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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