A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12585011



Internal ID2586827
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3611275
Supporting Variants
SamplesHG03228
Known GenesESR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12585011
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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