A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5927962



Internal ID8905365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:207667717..207672469hg38UCSC Ensembl
chr1:207841062..207845814hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg384753
hg194753
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676306
Supporting Variants
SamplesNA18868
Known GenesCR1L
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5927962
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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