A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585550



Internal ID6973072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26976322..26980168hg38UCSC Ensembl
Innerchr1:26976822..26979668hg38UCSC Ensembl
Outerchr1:26975322..26981168hg38UCSC Ensembl
chr1:27302813..27306659hg19UCSC Ensembl
Innerchr1:27303313..27306159hg19UCSC Ensembl
Outerchr1:27301813..27307659hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg383847
hg193847
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9894198, essv9894199
SamplesHG02976, HG03097
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585550
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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