A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9625847



Internal ID14705787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:8110684..8110703hg38UCSC Ensembl
Innerchr6:8110680..8110707hg38UCSC Ensembl
Outerchr6:8110661..8110726hg38UCSC Ensembl
chr6:8110917..8110936hg19UCSC Ensembl
Innerchr6:8110913..8110940hg19UCSC Ensembl
Outerchr6:8110894..8110959hg19UCSC Ensembl
chr6:8055916..8055935hg18UCSC Ensembl
Innerchr6:8055939..8055912hg18UCSC Ensembl
Outerchr6:8055893..8055958hg18UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3340355
Supporting Variants
SamplesNA18969
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv9625847
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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