A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611323



Internal ID6998232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154617984..154631338hg38UCSC Ensembl
Innerchr6:154618134..154631188hg38UCSC Ensembl
Outerchr6:154617834..154631488hg38UCSC Ensembl
chr6:154939118..154952472hg19UCSC Ensembl
Innerchr6:154939268..154952322hg19UCSC Ensembl
Outerchr6:154938968..154952622hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3813355
hg1913355
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12593728
SamplesHG02881
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611323
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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