A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3330928



Internal ID15177916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35792297..35799495hg38UCSC Ensembl
Innerchr6:35793297..35798495hg38UCSC Ensembl
Outerchr6:35791297..35800495hg38UCSC Ensembl
chr6:35760074..35767272hg19UCSC Ensembl
Innerchr6:35761074..35766272hg19UCSC Ensembl
Outerchr6:35759074..35768272hg19UCSC Ensembl
chr6:35868052..35875250hg18UCSC Ensembl
Innerchr6:35869052..35874250hg18UCSC Ensembl
Outerchr6:35867052..35876250hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg387199
hg197199
hg187199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3491e59
Supporting Variantsessv8695290
SamplesNA19239
Known GenesCLPS
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3330928
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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