A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585102



Internal ID6625420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6302076..6307565hg38UCSC Ensembl
Innerchr1:6302088..6307553hg38UCSC Ensembl
Outerchr1:6302064..6307577hg38UCSC Ensembl
chr1:6362136..6367625hg19UCSC Ensembl
Innerchr1:6362148..6367613hg19UCSC Ensembl
Outerchr1:6362124..6367637hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg385490
hg195490
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9845893, essv9845892
SamplesHG03895, HG04107
Known GenesACOT7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585102
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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