A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3587868



Internal ID6975291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168619349..168621947hg38UCSC Ensembl
Innerchr1:168619349..168621947hg38UCSC Ensembl
Outerchr1:168619131..168622131hg38UCSC Ensembl
chr1:168588587..168591185hg19UCSC Ensembl
Innerchr1:168588587..168591185hg19UCSC Ensembl
Outerchr1:168588369..168591369hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg382599
hg192599
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10183200
SamplesHG01921
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3587868
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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