A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12199834



Internal ID5661268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15215018..15222820hg38UCSC Ensembl
Innerchr6:15215518..15222320hg38UCSC Ensembl
Outerchr6:15214018..15223820hg38UCSC Ensembl
chr6:15215249..15223051hg19UCSC Ensembl
Innerchr6:15215749..15222551hg19UCSC Ensembl
Outerchr6:15214249..15224051hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg387803
hg197803
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3608167
Supporting Variants
SamplesNA19072
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12199834
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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