A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610072



Internal ID6996991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96222408..96235539hg38UCSC Ensembl
Innerchr6:96222408..96235539hg38UCSC Ensembl
Outerchr6:96222279..96235659hg38UCSC Ensembl
chr6:96670284..96683415hg19UCSC Ensembl
Innerchr6:96670284..96683415hg19UCSC Ensembl
Outerchr6:96670155..96683535hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3813132
hg1913132
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12472491
SamplesNA18538
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610072
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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