A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611085



Internal ID6997996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:142906001..142908827hg38UCSC Ensembl
Innerchr6:142906051..142908777hg38UCSC Ensembl
Outerchr6:142905951..142908877hg38UCSC Ensembl
chr6:143227138..143229964hg19UCSC Ensembl
Innerchr6:143227188..143229914hg19UCSC Ensembl
Outerchr6:143227088..143230014hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg382827
hg192827
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12574638, essv12574637, essv12574644, essv12574646, essv12574639, essv12574641, essv12574645, essv12574642, essv12574640, essv12574643
SamplesHG03772, HG03885, HG03746, HG03693, HG02793, HG03786, HG03711, HG04093, HG03653, HG04056
Known GenesHIVEP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611085
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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