A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6042961



Internal ID9020364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:101227743..101233626hg38UCSC Ensembl
chr1:101693299..101699182hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg385884
hg195884
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662889
Supporting Variants
SamplesNA18870
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6042961
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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