A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609700



Internal ID6996620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:79802637..79808355hg38UCSC Ensembl
Innerchr6:79802654..79808339hg38UCSC Ensembl
Outerchr6:79802621..79808372hg38UCSC Ensembl
chr6:80512354..80518072hg19UCSC Ensembl
Innerchr6:80512371..80518056hg19UCSC Ensembl
Outerchr6:80512338..80518089hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg385719
hg195719
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12448719
SamplesHG02116
Known GenesC6orf7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609700
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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