A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670043



Internal ID9936148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:98726259..98737316hg38UCSC Ensembl
Outerchr1:98726222..98737366hg38UCSC Ensembl
Innerchr1:99191815..99202872hg19UCSC Ensembl
Outerchr1:99191778..99202922hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3811145
hg1911145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6404010
SamplesNA18874
Known GenesSNX7
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670043
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer