A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673027



Internal ID9592446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23679603..24432457hg38UCSC Ensembl
chr7:23719222..24472076hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38752855
hg19752855
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5918897
SamplesNA18986
Known GenesFAM221A, NPY, STK31
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673027
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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