A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608160



Internal ID6995090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15069278..15079707hg38UCSC Ensembl
Innerchr6:15069328..15079657hg38UCSC Ensembl
Outerchr6:15069228..15079757hg38UCSC Ensembl
chr6:15069509..15079938hg19UCSC Ensembl
Innerchr6:15069559..15079888hg19UCSC Ensembl
Outerchr6:15069459..15079988hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3810430
hg1910430
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12199817
SamplesHG00341
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608160
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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