A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3426257



Internal ID14926528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3776617..3776917hg38UCSC Ensembl
Innerchr6:3776617..3776917hg38UCSC Ensembl
Outerchr6:3776605..3777460hg38UCSC Ensembl
chr6:3776851..3777151hg19UCSC Ensembl
Innerchr6:3776851..3777151hg19UCSC Ensembl
Outerchr6:3776839..3777694hg19UCSC Ensembl
chr6:3721850..3722150hg18UCSC Ensembl
Innerchr6:3721850..3722150hg18UCSC Ensembl
Outerchr6:3721838..3722693hg18UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38301
hg19301
hg18301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8652335
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformSOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3426257
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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