A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3587153



Internal ID6974580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109660894..109674476hg38UCSC Ensembl
Innerchr1:109661044..109674326hg38UCSC Ensembl
Outerchr1:109660744..109674626hg38UCSC Ensembl
chr1:110203516..110217098hg19UCSC Ensembl
Innerchr1:110203666..110216948hg19UCSC Ensembl
Outerchr1:110203366..110217248hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3813583
hg1913583
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10056815, essv10056816
SamplesHG00436, HG00107
Known GenesGSTM2, GSTM4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3587153
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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