A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611275



Internal ID6651494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151944725..151959448hg38UCSC Ensembl
Innerchr6:151944738..151959435hg38UCSC Ensembl
Outerchr6:151944712..151959461hg38UCSC Ensembl
chr6:152265860..152280583hg19UCSC Ensembl
Innerchr6:152265873..152280570hg19UCSC Ensembl
Outerchr6:152265847..152280596hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3814724
hg1914724
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12585011
SamplesHG03228
Known GenesESR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611275
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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