A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12585015



Internal ID3782524
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3611276
Supporting Variants
SamplesHG03433
Known GenesESR1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12585015
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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