A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658206



Internal ID9924311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:205136965..205138935hg38UCSC Ensembl
Outerchr1:205136808..205139088hg38UCSC Ensembl
Innerchr1:205106093..205108063hg19UCSC Ensembl
Outerchr1:205105936..205108216hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg382281
hg192281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv92e199
Supporting Variantsessv6351303, essv5972544
SamplesNA19457, NA19449
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658206
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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