A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585746



Internal ID6973267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37166786..37221675hg38UCSC Ensembl
Innerchr1:37166843..37221619hg38UCSC Ensembl
Outerchr1:37166730..37221732hg38UCSC Ensembl
chr1:37632387..37687276hg19UCSC Ensembl
Innerchr1:37632444..37687220hg19UCSC Ensembl
Outerchr1:37632331..37687333hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3854890
hg1954890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9908806
SamplesNA19819
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585746
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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