A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12585989



Internal ID2587805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:152068854..152071100hg38UCSC Ensembl
Innerchr6:152068854..152071100hg38UCSC Ensembl
Outerchr6:152068854..152071100hg38UCSC Ensembl
chr6:152389989..152392235hg19UCSC Ensembl
Innerchr6:152389989..152392235hg19UCSC Ensembl
Outerchr6:152389989..152392235hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg382247
hg192247
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3611278
Supporting Variants
SamplesNA19152
Known GenesESR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12585989
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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