A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1007484



Internal ID6719598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:89161543..89161543hg38UCSC Ensembl
chr7:88790857..88790857hg19UCSC Ensembl
chr7:88628793..88628793hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3873
hg1973
hg1873
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3570403
SamplesHuRef
Known GenesZNF804B
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1007484
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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