A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3586908



Internal ID6974336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:98726239..98737334hg38UCSC Ensembl
Innerchr1:98726272..98737302hg38UCSC Ensembl
Outerchr1:98726207..98737367hg38UCSC Ensembl
chr1:99191795..99202890hg19UCSC Ensembl
Innerchr1:99191828..99202858hg19UCSC Ensembl
Outerchr1:99191763..99202923hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3811096
hg1911096
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10027063
SamplesNA18874
Known GenesSNX7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3586908
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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