A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6335956



Internal ID9313359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:45530922..45532849hg38UCSC Ensembl
chr2:45758061..45759988hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg381928
hg191928
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659564
Supporting Variants
SamplesNA11993
Known GenesSRBD1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6335956
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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