A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6174006



Internal ID8799456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:1455518..1456275hg38UCSC Ensembl
chr7:1495154..1495911hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38758
hg19758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2672441
Supporting Variants
SamplesHG00245
Known GenesMICALL2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6174006
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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