A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611276



Internal ID6998185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151982534..151990637hg38UCSC Ensembl
Innerchr6:151982684..151990487hg38UCSC Ensembl
Outerchr6:151982384..151990787hg38UCSC Ensembl
chr6:152303669..152311772hg19UCSC Ensembl
Innerchr6:152303819..152311622hg19UCSC Ensembl
Outerchr6:152303519..152311922hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg388104
hg198104
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12585022, essv12585027, essv12585024, essv12585023, essv12585026, essv12585020, essv12585019, essv12585013, essv12585014, essv12585021, essv12585017, essv12585018, essv12585015, essv12585012, essv12585016, essv12585025
SamplesHG03449, NA19315, HG01242, NA18908, HG02144, NA19118, NA19113, NA19395, NA19035, NA19375, HG02759, HG03433, NA19376, NA19185, HG03445, HG03439
Known GenesESR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611276
Frequency
Sample Size2504
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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