A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610504



Internal ID6997421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:117964720..117966844hg38UCSC Ensembl
Innerchr6:117964729..117966836hg38UCSC Ensembl
Outerchr6:117964712..117966853hg38UCSC Ensembl
chr6:118285883..118288007hg19UCSC Ensembl
Innerchr6:118285892..118287999hg19UCSC Ensembl
Outerchr6:118285875..118288016hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg382125
hg192125
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12516778
SamplesHG02485
Known GenesSLC35F1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610504
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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