A curated catalogue of human genomic structural variation




Variant Details

Variant: esv999577



Internal ID7082185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:101415877..101416985hg38UCSC Ensembl
chr7:101059158..101060266hg19UCSC Ensembl
chr7:100845878..100846986hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg381109
hg191109
hg181109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3583318
SamplesHuRef
Known GenesCOL26A1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv999577
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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