A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5807912



Internal ID9897735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156165023..156165918hg38UCSC Ensembl
chr7:155957717..155958612hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38896
hg19896
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2678479
Supporting Variants
SamplesNA20786
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5807912
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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