A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610403



Internal ID6997320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:112929248..112972448hg38UCSC Ensembl
Innerchr6:112929290..112972407hg38UCSC Ensembl
Outerchr6:112929207..112972490hg38UCSC Ensembl
chr6:113250450..113293650hg19UCSC Ensembl
Innerchr6:113250492..113293609hg19UCSC Ensembl
Outerchr6:113250409..113293692hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3843201
hg1943201
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12505800
SamplesHG03773
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610403
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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