A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10153171



Internal ID154987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156396404..156399209hg38UCSC Ensembl
Innerchr1:156396404..156399209hg38UCSC Ensembl
Outerchr1:156396229..156399389hg38UCSC Ensembl
chr1:156366196..156369001hg19UCSC Ensembl
Innerchr1:156366196..156369001hg19UCSC Ensembl
Outerchr1:156366021..156369181hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg382806
hg192806
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3587637
Supporting Variants
SamplesNA18573
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10153171
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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