A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610388



Internal ID6997305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:112101402..112103284hg38UCSC Ensembl
Innerchr6:112101402..112103284hg38UCSC Ensembl
Outerchr6:112101158..112103472hg38UCSC Ensembl
chr6:112422605..112424487hg19UCSC Ensembl
Innerchr6:112422605..112424487hg19UCSC Ensembl
Outerchr6:112422361..112424675hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381883
hg191883
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12505673
SamplesNA18916
Known GenesFAM229B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610388
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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