A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585370



Internal ID6625689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17526093..17536754hg38UCSC Ensembl
Innerchr1:17526093..17536754hg38UCSC Ensembl
Outerchr1:17525593..17537254hg38UCSC Ensembl
chr1:17852589..17863249hg19UCSC Ensembl
Innerchr1:17852589..17863249hg19UCSC Ensembl
Outerchr1:17852089..17863749hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3810662
hg1910661
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9876182
SamplesHG00452
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585370
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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