A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612691



Internal ID6999591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:29319760..29552314hg38UCSC Ensembl
chr7:29359376..29591930hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38232555
hg19232555
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12717057
SamplesHG02654
Known GenesCHN2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612691
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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