A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12177682



Internal ID2318101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2811223..2826193hg38UCSC Ensembl
Innerchr6:2811243..2826174hg38UCSC Ensembl
Outerchr6:2811204..2826213hg38UCSC Ensembl
chr6:2811457..2826427hg19UCSC Ensembl
Innerchr6:2811477..2826408hg19UCSC Ensembl
Outerchr6:2811438..2826447hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3814971
hg1914971
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3607915
Supporting Variants
SamplesHG02064
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12177682
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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