A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608656



Internal ID6995580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34356852..34364029hg38UCSC Ensembl
Innerchr6:34356852..34364029hg38UCSC Ensembl
Outerchr6:34356352..34364529hg38UCSC Ensembl
chr6:34324629..34331806hg19UCSC Ensembl
Innerchr6:34324629..34331806hg19UCSC Ensembl
Outerchr6:34324129..34332306hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg387178
hg197178
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12312815
SamplesNA19909
Known GenesNUDT3, RPS10-NUDT3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608656
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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