A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611295



Internal ID6998204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:153182707..153207918hg38UCSC Ensembl
Innerchr6:153182738..153207887hg38UCSC Ensembl
Outerchr6:153182676..153207949hg38UCSC Ensembl
chr6:153503842..153529053hg19UCSC Ensembl
Innerchr6:153503873..153529022hg19UCSC Ensembl
Outerchr6:153503811..153529084hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg3825212
hg1925212
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12589364
SamplesNA20503
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611295
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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