A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626358



Internal ID15849891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:156556628..156559143hg38UCSC Ensembl
Outerchr1:156526420..156528935hg19UCSC Ensembl
Outerchr1:154793044..154795559hg18UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg382516
hg192516
hg182516
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511716
Supporting Variants
Samples1
Known GenesIQGAP3
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626358
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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