A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12581299



Internal ID6294161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150322292..150326710hg38UCSC Ensembl
Innerchr6:150322293..150326710hg38UCSC Ensembl
Outerchr6:150322292..150326711hg38UCSC Ensembl
chr6:150643428..150647846hg19UCSC Ensembl
Innerchr6:150643429..150647846hg19UCSC Ensembl
Outerchr6:150643428..150647847hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg384419
hg194419
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3611230
Supporting Variants
SamplesNA19835
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12581299
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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