A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610308



Internal ID6650534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108060849..108071102hg38UCSC Ensembl
Innerchr6:108061349..108070602hg38UCSC Ensembl
Outerchr6:108059849..108072102hg38UCSC Ensembl
chr6:108382053..108392306hg19UCSC Ensembl
Innerchr6:108382553..108391806hg19UCSC Ensembl
Outerchr6:108381053..108393306hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3810254
hg1910254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12499509
SamplesHG02601
Known GenesOSTM1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610308
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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