A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3396658



Internal ID15243621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2773777..2773785hg38UCSC Ensembl
Innerchr6:2773769..2773791hg38UCSC Ensembl
Outerchr6:2773763..2773799hg38UCSC Ensembl
chr6:2774011..2774019hg19UCSC Ensembl
Innerchr6:2774003..2774025hg19UCSC Ensembl
Outerchr6:2773997..2774033hg19UCSC Ensembl
chr6:2719010..2719018hg18UCSC Ensembl
Innerchr6:2719024..2719002hg18UCSC Ensembl
Outerchr6:2718996..2719032hg18UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38259
hg19259
hg18259
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8927642, essv8927643, essv8927641, essv8927648, essv8927644, essv8927650, essv8927661, essv8927664, essv8927660, essv8927653, essv8927647, essv8927652, essv8927656, essv8927649, essv8927655, essv8927654, essv8927658, essv8927645, essv8927662, essv8927651, essv8927663, essv8927659, essv8927665
SamplesNA18947, NA18561, NA18507, NA11920, NA12004, NA12155, NA11992, NA19138, NA18498, NA19172, NA12828, NA18605, NA18579, NA18537, NA18566, NA11919, NA18856, NA18555, NA19225, NA18523, NA18570, NA18593, NA19147
Known GenesWRNIP1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3396658
Frequency
Sample Size185
Observed Gain23
Observed Loss0
Observed Complex0
Frequencyn/a


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