A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12626185



Internal ID521035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:164326941..164400741hg38UCSC Ensembl
Innerchr6:164326971..164400711hg38UCSC Ensembl
Outerchr6:164326911..164400771hg38UCSC Ensembl
chr6:164747974..164821774hg19UCSC Ensembl
Innerchr6:164748004..164821744hg19UCSC Ensembl
Outerchr6:164747944..164821804hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3873801
hg1973801
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3611594
Supporting Variants
SamplesHG00187
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12626185
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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