A curated catalogue of human genomic structural variation




Variant Details

Variant: esv994123



Internal ID7062918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:37186459..37196833hg38UCSC Ensembl
Outerchr9:37186456..37196830hg19UCSC Ensembl
Outerchr9:37176456..37186830hg18UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg3810375
hg1910375
hg1810375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564146
SamplesHuRef
Known GenesZCCHC7
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv994123
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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