A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564856



Internal ID7035956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:156556536..156560148hg38UCSC Ensembl
Outerchr1:156526328..156529940hg19UCSC Ensembl
Outerchr1:154792952..154796564hg18UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg383613
hg193613
hg183613
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv994163
Supporting Variants
SamplesHuRef
Known GenesIQGAP3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564856
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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