A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3587160



Internal ID6627467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109919663..109920393hg38UCSC Ensembl
Innerchr1:109919672..109920384hg38UCSC Ensembl
Outerchr1:109919654..109920402hg38UCSC Ensembl
chr1:110462285..110463015hg19UCSC Ensembl
Innerchr1:110462294..110463006hg19UCSC Ensembl
Outerchr1:110462276..110463024hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38731
hg19731
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10061171, essv10061180, essv10061178, essv10061170, essv10061174, essv10061179, essv10061177, essv10061175, essv10061169, essv10061173, essv10061172, essv10061176
SamplesHG01372, HG00100, NA20506, HG01935, HG02420, HG00125, HG00282, HG01351, HG01383, NA20534, HG01269, NA20513
Known GenesCSF1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3587160
Frequency
Sample Size2504
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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